Immune Response to Tick-Borne Hemoparasites: Host Adaptive Immune Response Mechanisms as Potential Targets for Therapies and Vaccines

Abstract

Tick-transmitted pathogens cause infectious diseases in both humans and animals. Different types of adaptive immune mechanisms could be induced in hosts by these microorganisms, triggered either directly by pathogen antigens or indirectly through soluble factors, such as cytokines and/or chemokines, secreted by host cells as response. Adaptive immunity effectors, such as antibody secretion and cytotoxic and/or T helper cell responses, are mainly involved in the late and long-lasting protective immune response. Proteins and/or epitopes derived from pathogens and tick vectors have been isolated and characterized for the immune response induced in different hosts. This review was focused on the interactions between tick-borne pathogenic hemoparasites and different host effector mechanisms of T- and/or B cell-mediated adaptive immunity, describing the efforts to define immunodominant proteins or epitopes for vaccine development and/or immunotherapeutic purposes. A better understanding of these mechanisms of host immunity could lead to the assessment of possible new immunotherapies for these pathogens as well as to the prediction of possible new candidate vaccine antigens.

1. Tick-Borne Hemoparasites and Interactions with Hosts

Ticks are considered to be second, worldwide, to mosquitoes as vectors of human diseases, but they are the most important vectors of disease-causing pathogens in domestic and wild animals [1,2]. Awareness on the impacts of tick-borne diseases is increasing [3], and they constitute a significant number of emerging infectious diseases [4].

The family Anaplasmataceae (order Rickettsiales) contains the tick-transmitted genera Anaplasma and Ehrlichia, infectious agents of companion, domestic and wildlife species, as well as of humans [5].

Anaplasma spp. is an obligate intracellular pathogen living inside host cells, protected from the host immune system. Anaplasma marginale, one of the most widespread pathogens of this genus, is the aetiologic agent of cattle anaplasmosis, a disease severely affecting the cattle industry [6]. The inflammatory disease results from the harmful response elicited by the host and it includes fever, anemia, weight loss, abortion, reduced milk production and, sometimes, death [7]. The zoonotic agent Anaplasma phagocytophilum, differently from A. marginale, does not replicate in erythrocytes but in circulating mature granulocytes and endothelial cells, causing high fever and leukopenia [8].

Ehrlichia spp. is an animal and human pathogen with public health importance [9]. The main Ehrlichia species with recognized zoonotic potential are Ehrlichia chaffeensis and Ehrlichia ewingii [10]. Ehrlichia species infect endothelial cells and white blood cells [10] and are able to survive in phagocytes, evading the immune response of the host and reprogramming the host cell defense mechanisms [11,12]. E. chaffeensis, one of the most investigated species, especially infects monocytes/macrophages, where it resides in an early endosome. E. chaffeensis survives in the host cell by inhibiting the fusion of phagosome and lysosome to evade destruction by lysosomal enzymes [13]. Both an excessive immune response against E. chaffeensis as well as a weak response in immunocompromised patients lead to a severe disease.

Rickettsia genus (family Rickettsiaceae, order Rickettsiales) includes an expanding number of species differing in antigenic and microbiological characteristics, ecology, distribution pathogenicity and association with arthropod hosts. Rickettsia species are traditionally classified into the Spotted Fever Group and the Typhus Group, with most of the known species belonging to the former [14]. At the site of arthropod inoculation, a localized rickettsial infection may be present as an eschar (“tache noir”). Following this, endothelial cells represent the primary targets for rickettsia infection since one of the main pathologic effects of rickettsial infection is increased vascular permeability. Disseminated infection may result in severe vasculitis and endothelial damage [15].

Among tick-borne protozoa, piroplasms of Babesia and Theileria genera are widespread pathogens causing economic losses worldwide. Babesia spp. (order Piroplasmida, family Babesidae) infects and multiplies inside erythrocytes, resulting in red blood cell lysis [16]. More than one hundred Babesia species exist and are able to infect a wide range of vertebrate hosts. In particular, cattle babesiosis, mainly due to Babesia bovis and Babesia bigemina, causes relevant economic losses in several countries. Infections with Babesia are also common in wild animals, although usually subclinical [17]. Babesiosis is also a zoonosis of increasing importance [18,19]. Infected hosts are able to develop immunity towards Babesia species, involving both humoral and cellular factors [16].

Theileria spp. (order Piroplasmida, family Theileridae) infects leukocytes at the sporozoite stage. Inside leucocytes, sporozoites multiply by merogony and then schizonts develop in merozoites that are released and invade red blood cells, forming piroplasms [20]. Theileria species infect domestic and wild animals; they can be gathered into schizont “transforming” or “non-transforming” species. Transforming parasites include species responsible for severe disease—among these are Theileria annulata (agent of tropical theileriosis) and Theileria parva (agent of East Coast fever) in cattle and Theileria lestoquardi (agent of malignant theileriosis) in small ruminants [21].

Non-transforming species, i.e., Theileria orientalis, Theileria mutans and Theileria velifera, are usually considered as benign but they also include pathogenic species [22]. Theileria parasites develop within the cytoplasm of host leukocytes, where the endosomal cell membrane dissolves, making the parasite not accessible to antibodies.

The comprehension of tick–host–pathogen interactions at the cellular and molecular levels, as, for example, the mechanisms regarding the immune response elicited in the host by the pathogen, is an essential issue for characterizing pathogen transmission, establishment and pathogenesis and for identifying novel checkpoints for pathogen control [2]. This review examines the interactions of the above-mentioned pathogens with different effector mechanisms of T- and/or B cell-mediated adaptive immunity, describing the efforts to define immunodominant proteins or epitopes for vaccine development and/or immunotherapeutic purposes.

2. Adaptive Immune Response to Antigens Derived from Tick-Transmitted Hemoparasites: A Useful Tool to Analyze Immunogenicity of Molecules

2.1. Anaplasma spp.

The outer membrane fraction of A. marginale is composed of at least six major surface polypeptides, which include the major surface proteins (MSPs) MSP-1a, MSP-1b, MSP-2, MSP-3, MSP-4 and MSP-5. Immunization with purified A. marginale outer membranes can induce complete protection against infection by homologous strains, probably due to CD4⁺ T-lymphocyte-mediated Interferon gamma (IFN-γ) release and secretion of immunoglobulin G (IgG)-2 antibodies against outer membrane protein epitopes. Protection against homologous challenge was shown in cattle immunized with purified A. marginale native MSP-1, MSP-2 and MSP-3, with significant reductions in anemia [23].

Recombinant proteins could be used as subunit vaccines to reduce the high costs of outer membrane purification and many types of nanoparticles have been already explored as nano-carriers for improving their immunogenicity. As an example, Pimentel and colleagues recently used carbon nanotubes as antigen delivery systems, taking advantage of nanotubes’ ability to protect the attached molecules against enzymatic degradation and to efficiently cross biological membranes [24]. The nanocomplex included the core motif of A. marginale MSP1a adsorbed onto the nanoparticle surface of a carbon nanotube. When the nanocomplex was used for mice immunization, it stimulated the production of IgG1 and IgG2a and increased the expression of pro-inflammatory (Tumor necrosis factor (TNF)-α; interleukin (IL)-12 and IL-18) and anti-inflammatory (IL-10) cytokines. Compared to the immunization with peptide-adjuvant, a balanced Th1 and Th2 immune response was induced.

Even a subcutaneous ear implant vaccine was developed for a slow release of the vaccine construct. A. marginale MSP1a was administered subcutaneously as priming, while a bio-erodible polyanhydride rod with intermediate slow release was used for boosting and the ear implant deposited subcutaneously was used to release antigen for a long time. The subcutaneous construct induced a durable protection against the pathogen, in particular when multiple adjuvants were used for antigen delivery [25].

Alternative subunit vaccines for A. marginale would include the use of subdominant proteins present in the outer membrane, showing the vantage of not changing during the infection and being highly conserved among different strains. They include the proteins of A. marginale type IV secretion system, a 1.05-MDa complex that spans the outer and inner bacterial membranes, whose role is mainly the host cell adhesion/invasion, and the elongation factor-Tu (Ef-Tu), a membrane-associated protein belonging to the family of hydrolases involved in protein synthesis [26]. Two other proteins of the A. marginale type IV secretion system, VirB9.1 and VirB9.2 induced a humoral and cellular immunity, stimulating CD4⁺ T-lymphocyte proliferation, IFN-γ secretion and IgG2 production in outer membrane-immunized cattle [27]. However, the vaccine based on the recombinant proteins VirB9.1, VirB9.2, VirB10, VirB11 and Ef-Tu was able to elicit high IgG2 titers in the immunized calves but failed to protect against A. marginale challenge. All the animals showed clinical symptoms and required treatments, suggesting that further studies are required to identify and express, in the native form, the main epitopes of these antigens [26].

A. phagocytophilum infection induces a mild immune suppression in humans and mice and the control is mediated in a CD4⁺ T cell-dependent mechanism. IFN-γ both aids in pathogen clearance and induces host pathology [28]. As for the other pathogens, the challenge is to find vaccine antigens able to cross-protect from many strains. The immunization carried out using the whole bacterium, indeed, did not protect the animals from an A. phagocytophilum infection [29].

2.2. Ehrlichia spp.

The role of CD4⁺ T cells in Ehrlichia infections has not yet been clarified as CD4 knockout (KO) mice have been reported to be capable of resolving E. chaffeensis experimental infection [30]. However, resolution of infection is increased or more rapid in the presence of CD4⁺ T cells both for E. chaffeensis and for E. ruminantium [31]. CD4⁺ T cells in Ehrlichia infection have shown to produce IFN-γ; in fact, IFN-γ KO mice were very susceptible to infection [32]. Interestingly, a combined depletion of IFN-γ and TNF-α showed a further detrimental effect on infection survival [33], suggesting a controlled interaction between such mediators in Ehrlichia infection.

In order to identify CD4⁺ Th1 epitopes inducing IFN-γ production, a screening of ten E. ruminantium proteins (Erum0660, Erum1150, Erum2540, Erum5420, Erum7140, Erum7320, Erum7350, Erum7360, Erum7620 and Erum8010) previously identified as immunogenic was carried out to determine their ability to induce cellular immunity in sheep [34]. The authors identified 23 peptides stimulating different cell-mediated immune responses. These peptides could efficiently induce memory CD4⁺ T cells to rapidly proliferate and significantly increase IFN-γ production in immune sheep Peripheral Blood Mononuclear Cells (PBMCs). The antigens represent possible vaccine candidates for inclusion in a multi-epitope vaccine that could overcome many limitations of the live blood vaccine for E. ruminantium, so far the only commercially available vaccine for this pathogen.

CD8⁺ T cells seem to be involved in the cross-regulation of IL-10 production during Ehrlichia infection. TNF-α promotes IL-10 production, which downregulates TNF-α expression [35]. The major role of CD8⁺ in the form of cytotoxic T-lymphocyte activity and/or gamma interferon production in experimental E. chaffeensis and E. muris infection remains to be elucidated [33]. In any case, CD8⁺ T cell-mediated tissue damage is related to fatal murine ehrlichiosis in association with TNF-α and IL-10 overproduction and CD4⁺ Th1 hyporesponsiveness [36].

Other Ehrlichia immune-reactive identified antigens include ferric ion-binding protein, disulfide bond formation protein, ankyrin repeat proteins (i.e., E. canis gp200), and tandem repeat proteins (TRP-) [37,38,39,40,41,42,43]. Several orthologs of TRPs have been discovered in E. chaffeensis and E. canis—for example, TRP120/TRP140, TRP75/TRP95, TRP47/TRP36 and TRP32/TRP19 [40]. Through interaction with several host proteins, TRPs contribute to the infection establishment. Antibodies against the most important TRPs in E. chaffeensis showed both in vitro inhibition of replication and in vivo reduction in bacterial load [44].

A recently identified E. muris TRP, P29, recognized as the ortholog E. chaffeensis TRP47 and E. canis TRP36, was found to generate a strong IgG antibody response and to stimulate CD4⁺ T cell differentiation into IFN-γ-producing Th1 effector/memory cells, activating macrophage microbicide activity. These effects suggest a possible inclusion for E. muris P29 in a subunit vaccine against ehrlichiosis [40].

Although antibodies are not generally effective during intracellular infections, Winslow and colleagues [45] reported an antibody role in E. chaffeensis infection control that was observed in both normal mice and mice with severe combined immunodeficiency (SCID). In particular, antibodies, usually IgG2, directed towards the bacterial Outer Membrane Proteins (OMPs), showed an elevated affinity and a long binding half-life. Probably, these antibodies stimulated the infected macrophages to kill and eliminate the phagocytized bacteria, inducing the expression by infected macrophages of different effector molecules, as inflammatory cytokines, reactive nitrogen intermediates, chemokines [46,47,48] by activating Fc Gamma Receptors. A second proposed action mechanism implies a role of the antibodies in bacteria opsonization during intercellular transfer, when the pathogen is exposed to their action.

Antibodies against Ehrlichia, OMPs P28-9 and P28-19 and heat-shock protein 60 were found to induce protection in mice [49,50]. Human monoclonal antibodies against E. chaffeensis OMP-1 were able to inhibit infection through both extracellular and intracellular effector mechanisms [51]. In particular, the methods proposed by the authors include a novel intracellular mechanism mediated by the tripartite motif protein 21 (TRIM21). The complex antibody E. chaffeensis, sensed by TRIM21, was able to initiate a significant pro-inflammatory response and recruit autophagic regulators and effectors, leading to rapid degradation of E. chaffeensis by selective autophagy. The results showed that humoral immunity in humans is effective against the intracellular pathogen E. chaffeensis, suggesting that these anti-E. chaffeensis human monoclonal antibodies could be potential candidates for immunotherapy.

A relevant role of liver and spleen as generative sites of B cell responses to E. muris in wild-type C57BL/6 carrier mice was recently investigated [52]. The authors found a proliferation of B cells within infected livers. Moreover, the occurrence of somatic hypermutation of B-cell clones was revealed by high-throughput sequencing of V regions, showing clonal mixing and trafficking between spleen and liver.

Regarding vaccination, no approved vaccine against E. chaffeensis infection is currently available. McGill and colleagues [53] recently proposed a potential vaccine candidate, showing that an attenuated mutant strain of E. chaffeensis, reporting a mutation in the Ech_0660 gene, was able to induce protection in dogs. The effect was observed not only when wild-type E. chaffeensis was intravenously administered [54] but also when the pathogen was tick-transmitted [53]. Ech_0660-vaccinated dogs produced antibodies against E. chaffeensis, and strong CD4⁺T cell responses and released a high IL-17 production, suggesting a possible role for IL-17 in the immune response to ehrlichial pathogens.

In a following study [55], the ability to protect from wild-type E. chaffeensis of another mutant organism, Ech_0230, was investigated, presenting defects in the capacity to replicate in vivo in the vertebrate host. However, unlike the Ech_0660 mutant, Ech_0230 vaccination with this second mutant did not protect the animals from subsequent wild-type challenge, probably due to the transient induced IgG response. The authors described, for the first time, in dogs infected with E. chaffeensis, a significant expansion of CD4⁺CD8⁺ double-positive T cells, whose role in immunity to persistent E. chaffeensis infection is not understood. This population undergoes clonal expansion and is involved in IFN-γ and IL-17 secretion and in the increase of granulysin and granzyme B production in response to E. chaffeensis antigen.

2.3. Rickettsia spp.

Studies on adaptive immunity and rickettsial infections have been closely related to scientific efforts for the identification of vaccine candidates, especially of T cell antigens potentially conferring cross-protection against different Rickettsia species.

Accumulating evidence in recent years has demonstrated a leading role of T cells in protection from Rickettsia infection, mainly via CD8⁺ T cells-mediated bacteria killing and CD4⁺ T cells that sustain protective immune reaction releasing effector factors [56]. As concerning CD8⁺ T cells, studies in experimental infections have proven that granzyme B enhanced expression, as well as IFN-γ production by CD8⁺ cells, induce Rickettsia killing [57]. Interestingly, CD8⁺-associated cytotoxic activity seems to be of evident importance in R. australis experimental infection but not in R. typhi infection [58]. Such an observation remarks that although cytotoxic activity is essential for Rickettsia killing, IFN-γ production by CD8⁺ cells is a relevant event contributing to limiting the infection from some Rickettsia species, as demonstrated in studies involving IFN-γ KO mice as CD8⁺ donors [59]. CD4⁺ T cells positively influence the activity of phagocytic cells in rickettsial infection [60]; major cytokines produced by activated CD4⁺ T cells in bacterial infections have been reported to be IFN-γ and TNF-α, related to a potentiated activity on nitric oxide-mediated killing by macrophages. However, it is worthy to note that CD4⁺ T cells may also develop in Th17 lineage, with production of IL-17A and IL-22 responsible for downstream regulation of a range of target cells [57]. Indeed, apart from stimulating nitric oxide (NO) production by macrophages, activated by IFN-γ, they orchestrate the promotion of further cytokine release from target tissue cells and immune phagocytic cells, thus sustaining the inflammatory environment for rickettsial killing. As for humoral immunity, the contribution of antibodies (Abs) on defense against rickettsial infection is still under investigation. The effects of immunization with Abs against rickettsia outer membrane proteins A and B have been evaluated in an experimental model of R. conorii infection, conferring protection mainly via opsonization mechanisms [61]. However, given the development of such Abs in a late infection phase, raising about 10–12 days after experimental infection, a possible involvement in secondary infections has been proposed. Instead, Ab anti-lipopolysaccharides appeared up to day 6 but their role and contribution in protection against rickettsia have been not established yet [62].

Since Rickettsiae need to proficiently exploit metabolite synthesis from host cells due to their condition of obligate intracellular bacteria, their effective survival strictly depends on successful invasion of host cells. Thus, Rickettsia surface cell antigens (sca) have been extensively recognized as key factors in adherence and invasion of target cells as endothelial and phagocytic cells. Sca family comprises 17 genes encoding proteins with a modular structure including an N-terminal domain, a central passenger domain and a C-terminal domain [63]; within sca family, five genes are conserved especially between Spotted Fever-Group Rickettsiae: sca0 (rOmpA), sca1, sca2, sca4 and sca5 (rOmpB). Apart from the demonstration of the protective action of Ab anti-OmpA or Ab anti-OmpB against R. conorii infection in experimental mice model [61], OmpB protein-derived synthetic peptides have been reported to positively influence CD8⁺ T cells, suggesting their potential in supporting adaptive immunity for vaccination purposes [64]. Moreover, the genes codifying these omp proteins contain both regions highly conserved among the different Rickettsia species as well as hypervariable regions, and for this reason, they are considered attractive targets for molecular detection and differentiation [65]. Other studies demonstrated the immune recognition of other Scas, as Sca1, Sca2 and Sca4 [63], although the contribution of each such protein in comparison with the most studied OmpA and OmpB still need to be established.

In an interesting study by Caro-Gomez et al. [66], a reverse vaccinology approach allowed for identifying potential antigens able to induce CD8⁺ T cells, CD4⁺ T cells or both. The R. prowazekii ORFeome has been analyzed in silico, identifying 100 and 85 rickettsial proteins displaying high-affinity binding peptides for Major Histocompatibility Complex (MHC) class I or class II (for CD8⁺ and CD4⁺ T cells activation, respectively); interestingly, 21 proteins contained peptides binding both to MHC classes I and II, suggesting their potential as vaccine candidates, by triggering both CD4⁺ and CD8⁺ T cell responses. Using an experimental mice model, it has been reported that five antigens (RP739, RP403, RP734, RP598 and RP778) conferred protection against R. typhi infection in mice via the stimulation of CD8⁺ T cells and IFN-γ-related production. Of interest, RP778 also promoted CD4⁺ T cells’ IFN-γ production, suggesting its ability to stimulate both CD4⁺ and CD8⁺ T cells. Although candidate antigens have been selected from the R. prowazekii ORFeome, protection was afforded towards R. typhi, suggesting a cross-protection between different Rickettsia species belonging to the Typhus Group. Furthermore, Caro-Gomez et al. [66] tested the potential of the same antigens to induce protection against R. conorii infection, resulting in 62.5% of mice being protected, in line with the protein similarity of ortholog antigens between R. prowazekii and R. conorii (73–90%). In addition, given that Rickettsiae have been also recognized as potential bioweapons, the definition of a successful vaccination strategy may represent an obligate challenge in the forthcoming years [67].

2.4. Babesia spp.

Host susceptibility to develop babesiosis has been related to genetic traits, as few murine strains (mainly C3H/HeJ) are susceptible to Babesia infections. Genetic tolerance was shown by Duangijnda et al. [68], who found increased frequencies of bovine leukocyte antigens (BoLA) in animals infected by Babesia spp. and A. marginale.

Cytokines may modulate the pathogenicity of Babesia spp. as, for example, IFN-γ production was not found in PBMC supernatant from Babesia sp. BQ1 (Lintan)-infected sheep. On the contrary, IFN-γ production was detected in B. divergens-infected sheep. The inverse occurred for IL-10, suggesting an important role for IFN-γ and IL-10 in sheep infections caused by these two pathogens. Indeed, IFN-γ produced during B. divergens infection may have a protective role, explaining the weak infectivity of B. divergens in sheep. In contrast, IL-10 was produced early during Babesia spp. BQ1 (Lintan) infection, and this could be responsible for the absence of IFN-γ production and the higher pathogenicity of this Babesia species in sheep [69].

Immunity derived by spleen cells was analyzed for its role in resolution of B. microti infection. Mice experimentally infected with B. microti showed significant splenic B- and T cell depletion and an increase in macrophage levels, suggesting their relevancy for disease resolution. Infected mice also showed significantly higher plasmatic concentration of CD4+ Th1 cells-secreted cytokines, such as IL-2 and IFN-γ. Thus, Th1 cell-mediated immunity appears to be important in the clearance of this intracellular pathogen. A significant increase was measured for IL-6, promoting differentiation of Th17 cells, while only moderate variations were observed for other Th17 cell-produced cytokines, such as IL-17A, IL-17F, IL-21 and IL-22 [70].

As concerning Babesia spp. immunogenic proteins, it was reported that B. bovis small heat shock protein (Hsp20) is recognized by CD4⁺ T lymphocytes from cattle that recovered from infection and immune to challenge. The protein shows a predicted amino acid sequence conserved among different B. bovis strains. Immune cattle were stimulated with truncated recombinant Hsp20 and overlapping peptides to define the location of CD4⁺ T-cell epitopes for possible inclusion in vaccines. Both amino-terminal (amino acids 1 to 105) and carboxyterminal (amino acids 48 to 177) regions resulted immunogenic, stimulating a strong T-cell proliferation and IFN-γ production. Moreover, amino acids from 11 to 62 of Hsp20 induced a T-cell response in animals with different MHC haplotypes [71].

Another investigated protein, B. bovis Rhoptry-associated protein 1 (RAP-1), is recognized by B- and T lymphocytes from cattle that recovered from infection and were immune to subsequent challenge and it could represent a possible vaccine candidate for B. bovis and B. bigemina bovine infections. Immunization with either the native or recombinant protein reduced parasitemia in challenged animals. An N-terminal portion of B. bovis RAP-1 containing immunodominant T-cell epitopes was used as a vaccine in combination with IL-12 and RIBI adjuvant to induce a type 1 response, in order to verify if it would prime calves for antibody and T-helper cell responses. RAP-1-specific IgG titers, T-lymphocyte proliferation and IFN-γ production were observed following inoculations of either recombinant full-length or the N-terminal portion of RAP-1. However, in spite of the presence of strong RAP-1-specific IgG and CD4⁺ T-lymphocyte responses, neither antigen stimulated a protective immune response [72].

The major surface antigen of B. microti merozoites (BMSA) was also evaluated as a potential vaccine candidate. The BMSA-induced immune response significantly inhibited pathogen invasion of the host erythrocytes and in vivo parasite growth. The protection was associated to the increase in the Th17 cytokine IL-17, the Th1 cytokine IL-12p70 and Th2 cytokines, such as IL-4 and IL-10. Ingenuity pathway analysis showed that IL-17 facilitated the secretion of Th2 cytokines, stimulating a Th2 response and promoting the high level of IgG1 expression. Furthermore, anti-BMSA monoclonal antibodies were able to confer protection to NOD/SCID mice from a challenge with B. microti [73].

Apical Membrane Antigen-1 of Babesia divergens (BdAMA-1) has been also analyzed as a vaccine candidate by evaluating its polymorphism and studying the humoral response against BdAMA-1 in sheep experimentally infected with B. divergens. Two BdAMA-1 haplotypes (A and B) were defined based on two nonsynonymous point mutations. Prediction of linear epitopes showed very similar antigenicity of the two haplotypes. Antibody production against the extracellular domain of BdAMA-1 is weak and late and it includes both IgG1 and IgG2. These results indicate that even if BdAMA-1 may not be an immunodominant antigen, it could induce a mixed type 1 and type 2 immune response [74]. AMA-1 orthologs have been also reported in other Babesia species [75,76,77,78].

AMA-1 proteins interact with the rhoptry neck protein 2 (RON2), which integrates to the red blood cell membrane after its secretion from the rhoptries in a complex formed with other RON proteins. For such reasons, a possible role of vaccine candidate for RON2 in Babesia species has been evaluated and a highly conserved gene encoding for RON2 was reported in B. bovis [79]. In this study, the authors designed and chemically synthesized four conserved peptides, containing predicted B-cell epitopes in hydrophilic regions of this protein. Antibodies anti-RON2 generated towards these peptides were able to recognize intraerythrocytic merozoites of B. bovis. Two of these peptides were also able to induce partially neutralizing antibodies that blocked the invasion process, as observed in the in vitro neutralization assays. Even in B. bigemina [80], RON2 is expressed in merozoites and contains conserved B-cell epitopes inducing neutralizing antibodies in naturally infected cattle.

A recombinant modified vaccinia virus Ankara vector expressing a chimeric multi-antigen comprehending Merozoite Surface Antigen—(MSA) 2c, RAP-1 and Hsp20 was obtained and evaluated as a vaccine candidate [81]. The chimeric multi-antigen comprises immunodominant B- and T cell regions of three B. bovis proteins and it was used to immunize mice in homologous and heterologous prime-boost with a recombinant protein cocktail. The best results were obtained by combining a prime of a protein cocktail and a boost with the recombinant virus. This protocol induced a high level of specific IgG antibodies and secreted IFN-γ and activation of IFN-γ⁺-, CD4⁺- and CD8⁺-specific T cells. In a following study, it was investigated if the use of adenoviral vectors as antibody-triggering agents would increase humoral immune responses. Results in mice confirmed that adenoviruses, as well as the bacterially expressed multi-antigen, are highly reliable primer candidates, inducing high percentages of CD4⁺ and CD8⁺ T cells with a Th1 cytokine profile [82]. Subsequently, the same authors [83] used this subunit vaccine as a prime to immunize 13–15-month-old Holstein-Friesian steers with a modified vaccinia Ankara vector as a boost. Both prime and boost expressed a chimeric multi-antigen including the immunodominant B and T cell epitopes of the three aforementioned B. bovis proteins (MSA–2c, RAP-1 and hsp20). Response to the new vaccine was compared with the one to B. bovis live attenuated vaccine used in Argentina (R1A). After the immunization, all bovines were inoculated with a virulent B. bovis strain. Both groups of vaccinated animals developed high titers of total IgG antibodies and an antigen-specific Th1 cellular response before and after the challenge. However, steers immunized with the subunit vaccine showed clinical signs of disease, indicating a lack of protection with this recombinant formulation and that further improvements are needed to achieve the desired effectiveness.

As concerning the role of B cells, it was reported that following B. microti infection, B cells secrete IL-10 and that naive B cells stimulated in vitro with B. microti produced high amounts of IL-10 [84]. This study showed that B cells sorted from B. microti-infected mice produced higher IL-10 levels in response to LPS stimulation than B cells sorted from naive mice. B cell-deficient mice developed significantly lower levels of parasitemia after B. microti infection and exhibited lower levels of serum IL-10 compared to wild-type mice, suggesting that IL-10-producing B cells may play a role in susceptibility to B. microti. These IL-10-producing B cells, also known as Bregs, were identified in experimental models of autoimmune diseases, cancer and helminth infections. In the same study, it was observed that the number of IL-10-producing CD1d high CD5⁺ Bregs significantly increased during the acute phase of B. microti infection, suggesting that these cells have a critical role in the susceptibility to the pathogen. B. microti-induced Bregs are associated with the induction of CD4⁺CD25⁺ FoxP3⁺ regulatory t-cells, also known as Tregs. More specifically, the frequency of CD4 ⁺CD25⁺FoxP3⁺ Tregs increased in concomitance with the IL-10-producing Breg development, while Treg induction by B. microti infection did not occur in the absence of IL-10-producing Bregs. These observations suggest that the anti-infective immunity could modulate many immunopathologies through different mechanisms comprising induction of T- and/or B regulatory cells [85].

2.5. Theileria spp.

The intracytoplasmic location favors cell-mediated immune responses and, in particular, immune recognition by CD8⁺ T cells of parasite proteins released into the host cell and exposed through the class I MHC. Many Theileria species are able to, in vitro, transform mononuclear leukocytes into continuously dividing cells, expressing surface MHC classes I and II [86] that have been extensively used in studies of CD8⁺ T cell responses [87]. Nevertheless, how they kill parasitized cells is still poorly known. As already reported for human and murine CD8⁺ T cells, and also in bovine, probably, CD8⁺ T cells act through granule exocytosis and, specifically, granzyme B [88]. Cytotoxic T lymphocytes (CTLs) usually elicit responses restricted to the parasite strain and this is related to the issue of cross-protection towards different strains.

Studies about antigenic variability among T. parva strains suggest that such cross-protection is incomplete [89]. For this reason, a combination of parasites derived from three T. parva isolates, known as the “Muguga cocktail”, is administered to confer a broader protection. However, some findings showed no substantial differences in CTL response following immunization with only the Muguga strain in comparison with the cocktail [90]. The analysis of CTL responses in animals of the same MHC I haplotype immunized with the Muguga cocktail showed a differential recognition of autologous cells even between haploidentical animals.

The preferential induction of responses to particular antigens is due to the presence of T cells with high-avidity receptors for the respective epitopes [91,92]. However, in purified populations of bovine naive CD8⁺ T cells cocultured with autologous T. parva-infected lymphoblasts, a specific CTL activity was observed only in the presence of specific CD4⁺ T cells. The presence of non-specific CD4⁺ T cells or cytokine preparations maintained the helper function only for immune, not naive, CTL cells [93].

Possible vaccine candidate antigens specific for CD8⁺ T cells (

Table 1. Overview of the main candidate vaccine antigens with the related immune response induced for each pathogen.

Pathogen	Protein	Immune Response Induced	References
Anaplasma spp.	Native Major Surface Protein-1 (MSP-1), MSP-2 and MSP-3 outer membranes	CD4+ T lymphocyte and Immunoglobulin G2 responses	[23]
	A. marginale MSP1a + carbon nanotubes	Production of IgG1 and IgG2a, increases in pro-TNF-α, IL-12, IL-18 and IL-10 cytokines	[24]
	A. marginale type IV secretion system proteins, VirB9-1 and VirB9-2	CD4+ T-lymphocyte proliferation and IgG2 production	[27]
Ehrlichia spp.	E. ruminantium peptides from Erum0660, Erum1150, Erum2540, Erum5420, Erum7140. Erum7320, Erum7350, Erum7360, Erum7620 and Erum8010	Stimulation of memory CD4+ T cells proliferation and IFN-γ production in immune sheep Peripheral blood mononuclear cell (PBMCs)	[34]
	Outer Membrane Proteins (OMPs) - P28 (OMP-1) - P28-9 (OMP-1g) - P28-12 - P28-19	- Specific IgG2a release - Protection in vivo	[49,50,51]
	Tandem Repeat Proteins (TRPs) - E. chaffensis/E. canis orthologs RP120/TRP140, TRP75/TRP95, TRP47/TRP36 and TRP32/TRP19	- Epitope-specific antibody (Ab) release, mainly IgG1 - Inhibition of Signal transducer and activator of transcription 1 (Stat1), Janus Kinase 1 and 2 (Jak1 and Jak2) phosphorylation induced by IFN- γ (for TRP47) - Replication inhibition in vitro - Reduction in bacterial load in vivo	[37,38,39,40,41,42,43,44]
	- E. muris ortholog P29	- Strong IgG antibody response - IFN-γ expression in CD4+ T cells, activating macrophage microbicidal activity	[40]
	Ankyrin repeat proteins - E. chaffeensis Ank200	- Specific antibodies release - TNF-α induction - Modulation of expression of Jak/Stat genes	[42]
	Heat-shock protein 60 (Hsp60/GroEL)	- Specific antibodies release - Protection in vivo	[50]
	- Ferric ion-binding protein (Fbp)	- Specific antibodies release	[38]
Rickettsia spp.	Surface Cell Antigens (Sca) - OmpA - OmpB	- Production of opsonising Abs promoting phagocyte-dependent killing of Rickettsiae - Protection from experimental R. conorii infection	[61,63,64]
	Candidate antigens from R. prowazekii - RP739 - RP403 - RP734 - RP598 - RP778	- Development of CD8+ T cells expressing IFN-γ - Protection from experimental R. typhi and R. conorii infection (cross-protection)	[66]
	RP778	- IFN-γ expression in CD4+ T cells	[66]
	RP778	- IFN-γ expression in CD4+ T cells	[66]
Babesia spp.	Rhoptry-Associated Protein (RAP-1)	Antigen-specific IgG and IFN-γ release	[72]
	Heat-shock protein 20 (Hsp 20)	T cell proliferation and IFN-γ production	[71]
	B. microti surface antigen (BMSA)	Th17 and Th2 activation and IgG1 secretion	[73]
	B. divergens Apical Membrane Antigen-1 (BdAMA-1)	IgG1, IgG2, Th1 and Th2 activation	[74]
	B. bovis rhoptry neck protein 2 (RON2)	Induction of partially neutralizing antibodies that blocked the invasion process	[79]
	Chimeric multi-antigen	Antigen-specific IgG1, CD4+ and CD8+ IFN-γ+	[81,82,83]
Theileria parva	Tp1–Tp2–Tp4–Tp5–Tp7–Tp8	CD8+ T-cell responses	[92,94,95,96,97,98,99,100,101]
	p67	Ab production	[102]
	Polymorphyc immunodominant molecule (PIM)	Production of Ab with neutralizing activity	[103,104]
	p150	Ab production
Theileria annulata	Ta5–Ta9–Ta11	CD8+ T-cell responses	[105]
	SPAG-1	Induction of IL-4-producing T-cells	[106]
	Tams1	Ab production	[107]
	TaSP (homologue of T. parva PIM)	Production of neutralizing Ab	[108]
Theileria orientalis	Major piroplasm surface protein (MPSP)	Ab production	[109,110,111,112,113,114,115]
Theileria lestoquardi	Tl8 –Tl9	CD8+ T-cell responses	[116]

) have been identified in T. parva [94,95,96,97] and nine promising epitopes in six T. parva antigens were identified, together with their respective BoLA MHC class I restriction elements [92]. Among these antigens, Tp1 and Tp2 are hypothetical proteins of unknown function, Tp7 is an Hsp90, Tp4 is the ε subunit of T-complex protein 1 and Tp5 and Tp8 have been identified as the elongation translation initiation factor 1A and a cysteine protease, respectively. Some of these antigens, in particular in Tp1 and Tp2, show a polymorphic variability [98,99,100]. Tp1 inoculated in cattle promoted survival at lethal doses of the pathogen and increased percentages of memory lymphocytes, confirming a promising role of this antigen for subunit vaccine development [101].

Animals subjected to repeated T. parva sporozoite challenge showed antibodies able to neutralize sporozoites in vitro [117], with most of them recognizing the sporozoite surface protein p67 of T. parva [102]. Subunit vaccination using a recombinant p67 elicited levels of protection up to 70% [118].

The polymorphic immunodominant molecule (PIM) expressed in T. parva sporozoites and schizonts is a target for murine monoclonal antibodies with neutralizing activity [103]. PIM causes a strong humoral response and is employed in a diagnostic ELISA [104].

Other T. parva antigens include the p150 antigen and the major merozoite/piroplasm surface antigen of 32 kDa. The first, a polymorphic antigen with variability in a region of repeated sequences, is recognized by recovery sera, expressed in sporozoite microspheres and, at low levels, in schizonts [119]. The second one induces high titers of specific antibodies in cattle but fails in conferring protection against the pathogen [120].

T. annulata elicits different adaptive immune responses [121,122] and stimulates cytokine release to favor presentation of parasite antigens to CD4⁺ T cells. These cells produce IFN-γ that acts on non-infected macrophages, activating their production of TNF-α and nitric oxide (NO), which destroy the infected cells. CD8⁺ T cells kill infected leukocytes, recognizing parasite MHC-presented antigens. The clinical signs and pathological lesions of the disease are caused by overproduction of cytokines [123], dissemination of transformed macrophages through the lymphatic system and other organs [124] and a dysregulated immune response [125].

B cells are arrested in the draining lymph nodes and do not differentiate, probably due to the elevated levels of IFN-γ. This inhibition may be a pathogen mechanism to change the uncontrolled Th1 responses observed both in vivo and in vitro [106,126].

T. annulata-infected macrophages acquire aberrant phenotype and show dendritic cell features, including enhanced antigen-presenting capabilities [127,128,129]. Moreover, the pathogen polyclonally activates naive T cells in a non-specific, superantigen manner [106,126] with loss of CD2 expression on the T cell surface [130], disrupting the normal T lymphocyte response and subsequent protective immunity [131]. Such a process is considered as the T. annulata immune evasion strategy. Tolerant cattle show less lymph node enlargement following T. annulata infection, related to a decreased proliferation of macrophages and T lymphocytes and the development of an appropriate immune response and recovery [132,133]. CD4⁺ T cell activation preceded that of CD8⁺ T cells, which shows a biphasic trend, with the first phase directed against MHC antigens of the immunizing cell line, and the second one, MHC class I-restricted, associated with a parasite-specific immune response [134]. For example, WC1⁺ gamma/delta TcR⁺ T cells recognize a surface determinant on T. annulata-infected cells but they need a second signal to proliferate, which can be provided by exogenous IL-2. Infected cells express cytokine transcripts encoding IL-1 alpha, IL-1 beta, IL-6 and TNFα, as well as IL-10, IL-12, IL-15 and type I interferons, but not IFN-γ, IL-2, IL-4 and IL-7 [106,135]. Among interferons, only type I IFN, in particular IFN-β, is expressed [86].

T. annulata antigens Ta5 and Ta9, the orthologs of T. parva Tp5 and Tp9, are recognized by CD8⁺ T cells, while a third antigen, not previously identified in T. parva, has been named Ta11 [105]. Another highly investigated T. annulata candidate is the major surface sporozoite antigen, SPAG-1, a 92-kDa protein containing elastin repeats. Antibodies towards its C-terminus inhibit sporozoite entry, even if SPAG-1-specific T cell lines were IL-2 dependent and produced IL-4 but not IFN-γ, suggesting that the induced immune response may require additional factors to be effective [106]. The major merozoite piroplasm surface antigen, a 32-kDa antigen also known as Tams1, is a prominent serological determinant of T. annulata, highly polymorphic among and within parasite isolates [107].

Both SPAG-1 and Tams1 confer partial protection using different delivery systems and adjuvants, but their antigenic diversity in parasite strains restrict their effectiveness as vaccine candidates [136].

A T. annulata surface protein (TaSP) is recognized by sera of cattle that recovered from infection. The protein, considered the T. annulata homologue of T. parva PIM, is expressed in the sporozoite and schizont stages [108].

T. orientalis do not transform leukocytes and the pathogenic phase is due to erythrocyte destruction and anemia. The immune response is largely cell-mediated, and the role of the humoral response is not very clear [137]. Moreover, although enlarged cells containing schizont-like structures have been identified in infected cattle [138], details of schizont development are unclear [139]. The spleen shows a relevant role in the acute infection [140] and it may be also involved in the serological response via the white pulp [137]. It is unknown whether acutely T. orientalis-infected animals become refractory to subsequent disease.

T. orientalis major piroplasm surface protein (MPSP), the ortholog of T. parva p32 and T. annulata Tams-1 [109], is highly expressed during both the sporozoite [110] and piroplasm phases [111,137] and it includes determinants for humoral and cellular immunity [112,113]. The IgG response to this protein correlated to clinical signs, parasite genotype and infection intensity [138]. This antigen has also been considered as a vaccine candidate [112] and two CD4⁺ T cell epitopes were detected showing amino acid substitutions among field variants [113]. Despite high antibody titers against MPSP in persistently infected cattle, host humoral immunity against MPSP is insufficient to completely control the infection [112] and, furthermore, antibody response against MPSP can be type-specific [114,115].

A T. orientalis gene with weak homology to Tp9/Ta9 was reported but its role in CTL response has not been clarified yet [109].

As concerns T. lestoquardi, mechanisms involved in protective immunity against the pathogen are still unknown [141,142]. Two T. lestoquardi proteins, Tl8 (putative cysteine proteinase, 349 aa) and Tl9 (hypothetical secreted protein, 293 aa), orthologs of T. parva and T. annulata genes, were identified as possible vaccine candidates. These antigens are recognized by in vitro CD8⁺ T cell lines, suggesting a possible involvement in protective T cell responses in vivo against T. lestoquardi-infected leukocytes [116].

3. Conclusions

Host immune response could interact with Babesia spp., Rickettsia spp., Anaplasma spp., Erlichia spp. and Theileria spp. using different cells and/or molecules responsible for innate or adaptive immunity. The protective effects on infectious diseases by different branches of immunity are related to the phases of the infection. Effector mechanisms of innate immune responses, rapidly displayed by the host, are able to inhibit the symptoms of the acute phase of infections [143], while the T- and B cell responses, mounted by the immune system after a while, are able to induce a long-term protection against pathologies induced by hemoparasites. Many different molecules are able to induce T- and/or B cell responses and could be considered as candidate vaccine antigens (Table 1). However, as recently proposed, the combination of tick-derived and pathogen-derived antigens would result in more effective and safe vaccines [144,145,146]. To further advance in this direction, the quantum vaccinomics approach based on the combination of protective epitopes or immunological quantum will allow for the design of regional and host/tick species-driven interventions for vaccine formulation and implementation [147,148]. Intriguingly, tick-transmitted pathogens could exert the modulation of autoimmune as well as allergic disorders, as demonstrated in different models of helminth infections. In conclusion, the immune response to pathogens transmitted by tick bites activates various effector mechanisms of innate and adaptive immunity, able to induce different types of protective or deleterious side effects for the host, such as autoimmune or allergic disorders. Different immunization routes and vaccine formulations offer promising perspectives for the control of tick-borne diseases while reducing side effects promoted by protective immunity.