key: cord-0844065-gwj9m6xa
authors: Ning, Zhaochen; Liu, Keyan; Xiong, Huabao
title: Roles of BTLA in Immunity and Immune Disorders
date: 2021-03-29
journal: Front Immunol
DOI: 10.3389/fimmu.2021.654960
sha: c29b6692c9c8dab6f21d7207bfddfb442a98c22b
doc_id: 844065
cord_uid: gwj9m6xa

B and T lymphocyte attenuator (BTLA) is one of the most important cosignaling molecules. It belongs to the CD28 superfamily and is similar to programmed cell death-1 (PD-1) and cytotoxic T lymphocyte associated antigen-4 (CTLA-4) in terms of its structure and function. BTLA can be detected in most lymphocytes and induces immunosuppression by inhibiting B and T cell activation and proliferation. The BTLA ligand, herpesvirus entry mediator (HVEM), does not belong to the classic B7 family. Instead, it is a member of the tumor necrosis factor receptor (TNFR) superfamily. The association of BTLA with HVEM directly bridges the CD28 and TNFR families and mediates broad and powerful immune effects. Recently, a large number of studies have found that BTLA participates in numerous physiopathological processes, such as tumor, inflammatory diseases, autoimmune diseases, infectious diseases, and transplantation rejection. Therefore, the present work aimed to review the existing knowledge about BTLA in immunity and summarize the diverse functions of BTLA in various immune disorders.

B and T lymphocyte attenuator (BTLA) is a member of the CD28 superfamily. Its gene is localized in the q13.2 region of chromosome 3 and consists of 5 exons with a total length of 870 bp. The protein structure of BTLA is similar to programmed cell death-1 (PD-1) and cytotoxic T lymphocyte associated antigen-4 (CTLA-4), which includes extracellular domain, transmembrane domain and cytoplasmic domain (1, 2) . The cytoplasmic domain contains growth factor receptorbound protein-2 (Grb-2) association motif, immunoreceptor tyrosine-based switch motif (ITSM), and immunoreceptor tyrosine-based inhibitory motif (ITIM). HVEM binding activates tyrosine phosphorylation of the ITIM in BTLA and leads to the recruitment of the Src homology domain 2 (SH2)-containing protein tyrosine phosphatases, SHP-1 and SHP-2, which generally mediate immunosuppressive effects (3, 4) . Interestingly, binding of the Grb-2 association motif with Grb-2 leads to the recruitment of PI3K protein subunit p85 and T cell activation (5). At present, herpes virus entry mediator (HVEM), which belongs to the tumor necrosis factor receptor superfamily, is the only identified ligand that can be detected in human cells (1) . HVEM can interact with BTLA in a cis or trans manner. On cells coexpressing BTLA and HVEM, BTLA can interact with HVEM in cis, whereas trans interaction occurs when BTLA and HVEM are expressed on different cells (2, 6) . In addition to BTLA, HVEM can also interact with CD160, lymphotoxin-a, LIGHT (TNFSF14), and synaptic adhesion-like molecule 5 (SALM5) (7-9). Notably, BTLA and CD160 compete for the same binding site within the CRD1/CRD2 region of HVEM, while LIGHT independently binds the opposite side of HVEM within the CRD2/CRD3 region (1, 8, 10) . BTLA can be extensively expressed in lymph nodes, thymus, and spleen, but little or no expression is detected in organs, such as the heart, kidney, brain, and liver (11). Among immune cells, BTLA is mainly expressed in B and T cells. In mouse spleen, the expression of BTLA is higher in B cells than T cells. With regard to T cells, BTLA expression can be detected on both CD4 + and CD8 + T cells, whereas CD4 + T cells express more BTLA than CD8 + T cells (12). Besides, its expression can also be detected in innate immune cells, such as dendritic cells (DCs) and monocytes (13). HVEM binding to BTLA exerts direct negative effects on the proliferation and activation of B and T cells (14) . As a result, they affect a variety of physiopathological processes. This review aimed to summarize the recent results on the effects of BTLA in regulating immune cell function and to explore its potential role in immune disorders.

BTLA and T Cells BTLA levels vary during T cell differentiation and activation processes. Specifically, BTLA is expressed in naive T cells, and the expression transiently increases upon activation, but is decreased in activated T cells (15) (16) (17) (18) . Moreover, the interaction manners between BTLA and HVEM also changes. Under homeostatic conditions, HVEM and BTLA interact in cis to provide intrinsic inhibitory signals. Upon T cell activation, HVEM is internalized, which allows BTLA to interact with HVEM in trans (6, 10). BTLA-deficient mice exhibit no defects in lymphocyte development, suggesting that BTLA is not necessary for T cell development (19). However, BTLA can significantly inhibit T cell activation and proliferation. BTLAdeficient T cells show increased proliferation (4) and are hyperresponsive to TCR-mediated activation (19). BTLA agonistic monoclonal antibody (mAb) suppresses the proliferation of T cells and the secretion of interleukin (IL)-10 and interferon g (IFN-g) upon anti-CD3 stimulation (20). Antibodies targeting BTLA enhance the proliferation of CD8 + T cells and blocking BTLA in combination with PD-1 is found to be effective in enhancing the exhausted human T cell response (21). Krieg et al. found that BTLA -/mice showed an elevated memory CD8 + T cell count and proposed that the increased T cell proliferation mediated by BTLA deficiency was associated with alterations in T cell memory subsets but not co-inhibition (22). However, Deppong et al. discovered that T cells with BTLA deficiency exhibited no enhanced proliferation, but showed decreased death (23). In addition, BTLA contributes to the induction of peripheral tolerance in CD4 + and CD8 + T cells (24). In naive T-cells, BTLA and HVEM form a cisheterodimeric complex, which blocks other co-signaling molecules from binding to HVEM and stimulating the NF-kB signaling pathway, thus maintaining the tolerance of T cells (6). BTLA engagement has been suggested to facilitate SHP-1 and SHP-2 recruitment (3, 4) . However, Chemnitz et al. reported that SHP-1 recruitment was not related to the function of BTLA, as blocking SHP-1 recruitment did not affect the function of BTLA (25). Paradoxically, it was recently shown that BTLA preferentially recruits SHP-1 to suppress T cell signaling more efficiently (26, 27). gdT cells can quickly produce inflammatory cytokines at sites of barrier to protect against pathogens. BTLA can limit gd T cell numbers and control proliferation and cytokine secretion in mature lymph node gd T cells (28). Vg9Vd2 cells are the main subset of gd T cells in peripheral blood that are reactive to tumors and microbial agents, and BTLA was found to be strongly expressed in resting Vg9Vd2 T cells. BTLA engagement inhibited Vg9Vd2 T cell proliferation, while targeting BTLA resulted in the enhancement of Vg9Vd2 TCR-mediated signaling (29).

BTLA in B cells has rarely been studied compared to that in T cells. In human B cell subsets, mature peripheral B cells display the most significant BTLA level, whereas a uniform BTLA expression is observed in naive, transitional, and memory peripheral B cells, and the lowest level is detected in bone marrow-derived precursor B cells (30). In addition, BTLA levels are downregulated in B cells of the aged, which is related to the decreased reactivity to the trivalent influenza vaccine (31). In mouse spleen, compared to T cells, B cells display higher surface BTLA level (12, 32). Consistent with its effect on the development of T cells, BTLA does not significantly affect the development of B cells, because normal growth of lymphocytes is detected in mice with BTLA deficiency (4, 19) . Moreover, it was found that BTLA/ HVEM ligation can suppress the functions of B cells (such as proliferation, cytokine secretion, and co-stimulatory molecule upregulation) (30, 33). Engagement of BTLA recruits SHP-1, leading to reduced activation of BCR downstream signaling molecules (30). However, Zhang et al. reported that BTLA antibodies had no effect on lipopolysaccharide (LPS)-or anti-IgM antibody-induced B cell proliferation in vitro (34). Regarding helper T (Th) cells, follicular Th (Tfh) cells represent the dominant subset that promotes antibody secretion by B cells. Mintz et al. discovered that HVEM engagement of BTLA on Tfh cells reduced T cell receptor (TCR) signaling and CD40 ligand mobilization to the synapse, thereby reducing the help to B cells and inhibiting B cell proliferation (35). Additionally, it was found that BTLA could inhibit IL-21 production by Tfh cells to suppress the development of germinal center B cells and subsequent IgG responses (36).

As its name implies, BTLA shows preferential expression in T and B cells, yet its expression can also be detected in additional immune cells, such as DCs. Immature DCs express lower levels of BTLA, and BTLA expression increases with maturation (37). The number of DCs in BTLA -/mice spleen was found to be similar to that in wild-type mice, suggesting that BTLA is not essential for DC development (38). The HVEM-BTLA pathway plays an important role in regulating DC homeostasis. The lymphotoxin b receptor signaling pathway triggers the proliferation of DCs, while the HVEM-BTLA signaling pathway suppresses DC proliferation, suggesting that the HVEM-BTLA pathway provides an inhibitory checkpoint for DC homeostasis (39). Xin et al. reported that BTLA overexpression suppressed DC maturation and enhanced the immune tolerance of immature DCs (40). BTLA can inhibit tolllike receptor 4 signaling and proinflammatory cytokine production in DCs, thereby inhibiting LPS-induced endotoxic shock (38). Jones et al. discovered that BTLA + DCs governed the conversion of peripheral Treg cells by upregulating CD5, thus enhancing the tolerance of peripheral Treg cells (41). Moreover, active pulmonary tuberculosis drives BTLA expression in DCs, thereby inhibiting Th17 and Th22 responses induced by DCs and promoting Treg and Th2 differentiation (42) . Further, urothelial cancer induces the overexpression of BTLA in DCs, resulting in reduced secretion of effector cytokines (43) .

BTLA is found to be expressed in tumor-infiltrating lymphocytes (TILs) and is often associated with impaired anti-tumor immune response. Upregulated BTLA expression in gallbladder cancer (GBC) plays a role in inhibiting anticancer immunity, and an increased proportion of BTLA + CD8 + cells is related to the unfavorable outcome of GBC patients (44) . In hepatocellular carcinoma (HCC) cases, the expression level of BTLA markedly increases in circulating CD4 + cells rather than in CD8 + T cells (45, 46) . Besides, blocking the BTLA/HVEM signaling pathway can promote IFN-g secretion by circulating CD4 + and CD8 + T cells (45) . BTLA + T cells show increased levels of additional checkpoint molecules, such as PD-1, lymphocyte-activation gene-3, T cell immunoglobulin and mucin-do-main-containing molecule-3 (TIM-3). In addition, these cells exhibit a poorly differentiated phenotype, reduced cytolysis, and increased proliferation potential among patients with diffuse large B-cell lymphoma (DLBCL). Further, increased BTLA levels are related to an advanced disease stage in DLBCL patients (47) . BTLA expression is elevated in T cells from patients with melanoma (48, 49) . Furthermore, PD-1 + TIM-3 -CD8 + T cells expressing BTLA are the largest tumor-specific CD8 + T cell subset among melanoma cases that show partial dysfunction with decreased IFN-g production compared with BTLA -T cells (49) . BTLA is highly expressed in type I NKT cells in murine autochthonous mammary tumors, and BTLA-neutralizing antibodies can inhibit tumor proliferation and pulmonary metastasis (50) . BTLA expression was also found to be upregulated in T cells from patients with lung cancer (51) . In addition, soluble BTLA (sBTLA) in plasma is significantly associated with the risk of death in patients with clear cell renal cell cancer, suggesting that sBTLA has a similar role to membranous BTLA in inhibiting T cell response (52) . However, some studies have reported contradictory results. For instance, as suggested by Song et al., BTLA levels decreased in colorectal cancer tissues in comparison with levels in matched non-carcinoma tissues. In addition, decreased BTLA levels predicted poor overall survival and less LNM (53) . Notably, BTLA is suggested to trigger both inhibitory and survival signaling, and may have a context-specific function in TILs (7). Although BTLA is a co-inhibitory receptor, higher frequencies and numbers of BTLA-expressing CD8 + TILs are markedly associated with positive adoptive cell therapy responses among melanoma cases (54) . This team further found that BTLA marks a less-differentiated TIL subset, which displays enhanced resistance to apoptosis and improved survival after tumor killing (55, 56) . Besides, growing evidence suggests that polymorphisms of BTLA increase susceptibility to a wide range of cancers. Rs1982809 is a functional single nucleotide polymorphism (SNP) that affects BTLA 3′-UTR activity and BTLA expression, and has been found to be associated with a higher incidence of renal cell carcinoma (57), chronic lymphocytic leukemia (58) and esophagogastric junction adenocarcinoma (59) . Five BTLA gene SNPs were found to be related to progesterone receptor, estrogen receptor, tumor size, p53, and C-erbB-2 statuses among Chinese females from the northeast Heilongjiang Province (60). However, Cao et al. found no significant relationship between BTLA polymorphisms and esophageal squamous cell carcinoma (61) .

BTLA negatively regulates T cell-mediated inflammation. BTLA -/mice experience a prolonged duration of allergic airway inflammation and enhanced recruitment of inflammatory cells relative to those in wild-type mice (62) . Moreover, DNFB-mediated contact hypersensitivity, CD8 + T cell proliferation, and IFN-g generation increased in BTLA -/mice, whereas these effects were reversed by an agonistic anti-BTLA antibody (63) . The BTLA + T cell frequency is elevated in the mucosa and blood of mice with colitis, and BTLA can control inflammatory responses by upregulating Foxp3 expression (64) . In a Con A challenge model of acute hepatitis, BTLA -/mice showed reduced survival and increased early secretion of serum cytokines, which was partly due to the negative regulation of NKT cells by BTLA (65) . Moreover, Shi et al. discovered that BTLA could induce the self-tolerance of CD8 + BTLA + T cells to reduce the attack on hepatocytes, thus regulating hepatic homeostasis in a Con A-induced hepatitis model in zebrafish (66) .

Notably, a growing body of research suggests that BTLA plays an important role in sepsis. Sepsis mortality is prevented in mice with BTLA deficiency, which presents with reduced leukocyte recruitment into the peritoneum, reduced IL-10 secretion, increased bacterial clearance, and suppressed neutrophil activation (67) . Besides, it is further found that critically ill sepsis patients show a markedly increased proportion of BTLA + CD4 + lymphocytes in peripheral blood, which is associated with a subsequent infection (68) . The BTLA level in Tregs (69) and plasma concentration of sBTLA (70, 71) are elevated in sepsis cases, and they are related to sepsis severity.

However, some studies have reported different results. Specifically, relative to that in normal subjects, the number of BTLA + CD4 + T cells decreased among patients with severe sepsis, and a lower percentage of BTLA + CD4 + T cells during the early stage of sepsis was associated with the severity and mortality of sepsis patients (72) . Furthermore, Spec et al. reported that differences in BTLA levels in CD4 + and CD8 + T cells were not statistically significant between patients with Candida sepsis and controls (73) . Interestingly, different clones of BTLA antibodies have two contradictory effects, including neutralizing and potentiating effects on BTLA-mediated signaling (74, 75) . Cheng et al. reported that BTLA antibody treatment increased the levels of cytokines and chemokines and promoted the recruitment of inflammatory cells into the peritoneal cavity, leading to deteriorated organ damage and increased mortality in mice with hemorrhagic shock/sepsis (76) . However, Kobayashi et al. found that a BTLA antibody rescued mice from LPS-induced endotoxic shock (38). The authors also suggested that mice with BTLA deficiency showed high susceptibility to LPS-induced endotoxic shock and that LPSmediated production of IL-12 and tumor necrosis factor a significantly increased in macrophages and DCs of mice with BTLA deficiency (38). These discrepant results from different studies may be related to the different functions of the antibodies used. Moreover, genetic variations in BTLA are associated with sepsis morbidity. In addition to increasing cancer susceptibility, Rs1982809 is also associated with the incidence of sepsis and multiple organ dysfunction scores (77) .

BTLA is suggested to play a vital role in the protection from autoimmunity. Mice with BTLA deficiency exhibit increased antigen-specific IgG responses and are sensitive to experimental autoimmune encephalomyelitis (EAE) (4, 78) . BTLA deficiency results in spontaneous development of autoimmune hepatitis-like disease, which is characterized by elevated transaminase levels, interface hepatitis, and hepatic spotty necrosis (79) . The number of BTLA-expressing B cells and CD19 + /BTLA + /IL-10 + cells obviously decreased in multiple sclerosis (MS) cases, while the remission of fingolimod-induced relapsed-remitted MS is related to a significantly increased number of CD19 + /BTLA + /IL-10 + B lymphocytes (80) . In patients with active systemic lupus erythematosus (SLE), the proportion of CD4 + BTLA + T cells is markedly decreased (81). Sawaf et al. found that in SLE cases, BTLA had a lower ability to suppress the activation of T cells, and such impaired BTLA function in lupus CD4 + T cells was found to be related to disease activity (82) . BTLA deficiency accelerates the lupus-like phenotype in autoimmune-prone MRL-lpr/lpr mice, and severe lymphocytic infiltration is detected in the lungs, kidneys, salivary glands, joints, and pancreas (83) . However, a study conducted in the Japanese population showed that there was no significant difference in haplotypes, genotypes, and alleles of the BTLA gene between SLE and healthy groups (84) . Anti-BTLA mAb treatment can delay the onset of autoimmune diabetes in non-obese diabetic (NOD) mice, increase the proportion of Tregs, and direct the cytokine milieu away from autoimmunity (85) . Transferring transgenic BTLA-expressing DCs into NOD mice markedly triggers the tolerance of CD8 + T cells, while attenuating the autoimmune diabetes severity (86) . In rheumatoid arthritis (RA) patients, BTLA-expressing CD3 + / CD4 + /CD8 + T cell proportions are remarkably increased, and the swollen joint count is negatively correlated with the percentage of BTLA + CD8 + T cells (87) . Lin et al. found that the C+800T SNP in the BTLA gene was associated with RA susceptibility (88) . Besides, the 590C SNP, a functional polymorphism of the BTLA gene, is markedly associated with RA susceptibility in the Japanese population (89) .

Since BTLA can provide both inhibitory and pro-survival signals to T cells, it plays a dual role during infection. BTLA expression increases in various infectious diseases, which is generally related to an impaired immune response against infection. BTLA is strongly upregulated in both CD4 + and CD8 + T cells from COVID-19 patients (90) . Similarly, BTLA levels increase in CD4 + and CD8 + T cells from patients with pulmonary tuberculosis, and this is related to disease progression (91) . During infection with primary cytomegalovirus (CMV), BTLA is highly induced in CD8 + T cells, and BTLA blockade enhances CMV-specific CD8 + T cell proliferation (92) . Increased BTLA level in intrahepatic lymphocytes is related to impaired T cell responses in the process of chronic hepatitis B virus (HBV) infection, whereas blocking BTLA promotes cytokine production and T cell proliferation (93) . In patients with chronic HBV infection, a subset of antigen-specific CD8 + T cells with low IFNg production express high levels of BTLA, and these cells play a vital role in the regulation of CD8 + T cell responses via BTLA signaling (94) . In patients with severe community-acquired pneumonia and in mice with acute lung inflammation, circulating BTLA + CD4 + lymphocyte proportions markedly increased, whereas agonistic anti-BTLA antibody reduced the activation of the NF-kB pathway and attenuated the inflammatory responses (95) . In mice infected with the parasitic nematode Strongyloides ratti, BTLA expression in CD4 + T cells was upregulated. Additionally, deficiency of either BTLA or HVEM leads to decreased amounts of adult parasites in the small intestine, while reducing the larval output in the process of infection (96) . Moreover, BTLA -/mice have also shown resistance to infection in several other disease models. During infection with murine hepatitis virus strain-3 (MHV-3), BTLA -/mice show markedly improved spleen and liver injuries and reduced mortality (97) . BTLA suppresses both the innate and T/B cell-dependent adaptive immune responses during experimental malaria, whereas BTLA -/mice show markedly decreased parasitemia, and early clearance of infections (98) . Furthermore, BTLA -/mice are more resistant to listeriosis infection (99), whereas targeting BTLA promotes primary and memory T cell responses (100) and accelerates early bacterial clearance (99) . Interestingly, BTLA -/mice have a decreased number of Listeria-specific CD8 + T cells, which reveals the dual effects of BTLA in regulating anti-intracellular pathogen responses in the host (100, 101) . Furthermore, HVEM expression in CD8 + T lymphocytes and BTLA expression in other cell types are necessary for the optimal survival of effector and memory T cells, suggesting that the BTLA/HVEM pathway enhances activated CD8 + T cell survival in the process of Listeria infection (101) . During vaccinia virus infection, BTLA or HVEM deficiency markedly damages the survival of effector CD8 + T cells and protective immune memory (102) . BTLA + ab T cells display a central memory phenotype to combat Mycobacterium tuberculosis (Mtb) infection, as manifested by increased cell proliferation and cytokine secretion, suggesting that BTLA expression in abT cells is involved in protective immune memory against Mtb infection among patients with active pulmonary tuberculosis (103) .

The inhibitory role of BTLA on T cells has also been supported by transplantation studies. BTLA can inhibit donor anti-host T cell responses and ameliorate graft-versus-host disease (GVHD) resulting from allogeneic bone marrow transplantation (104, 105) . In patients with acute renal allograft rejection, BTLA levels in peripheral CD3 + T lymphocytes are markedly lower than those in normal controls who show stable functions of the transplanted kidney (106, 107) . Agonistic anti-BTLA antibody treatment prolongs cardiac allograft survival in mice with increased CD4 + CD25 + Foxp3 + cells and reduced IL-2 and IFN-g production (108) . Furthermore, BTLA overexpression in a rat model can markedly suppress acute kidney rejection and extend allograft survival (106) . Partially MHC-mismatched allografts can potently induce BTLA expression, while targeting BTLA prompts rapid rejection (109) . Agonistic antiBTLA antibody combined with CTLA-4 immunoglobulin treatment can prolong the survival of islet allografts, while promoting indefinite graft acceptance (110, 111) . Moreover, according to the latest research, overexpression of BTLA combined with CTLA-4 in kidney transplant recipients reduced IL-2 production, suppressed T cell proliferation, improved graft function, attenuated acute T cell-mediated rejection, and extended graft survival (112) . However, there have been some contradictory reports. For example, Del Rio et al. reported that BTLA blockade alleviated acute GVHD reaction in an F1 transfer semiallogeneic murine model (113, 114) . Rodriguez-Barbosa et al. found that targeting BTLA/HVEM showed no effect on modulating graft rejection across a fully MHC mismatched barrier and that the donorspecific allogeneic immune response was independent of the HVEM/BTLA signaling pathway (115) . Besides, Wang et al. explored the role of BTLA and HVEM polymorphisms in antibody-mediated rejection in renal transplant recipients and found that none of the polymorphisms identified was associated with antibody-mediated rejection (116) .

BTLA has been found to affect the function of a variety of immune cells and plays an important role in many immunerelated diseases ( Table 1) . There is growing evidence that BTLA can provide both inhibitory and pro-survival signals to T cells. As a result, BTLA is found to play dual roles in tumor (7, 55, 56) and infection (101, 102) immunity, and the function of BTLA in related diseases may be context specific. BTLA can be expressed by numerous cell types. At present, the existing studies on BTLA mainly focus on T and B cells, and thus studies on the function of BTLA in other immune cells should be strengthened. Numerous clones of anti-BTLA antibodies have been developed, and the main antibody clones such as 6A6 and 6F7 were summarized in the review by Crawford and Wherry (75) . Studies have examined the role of anti-BTLA antibodies in tumor, inflammatory diseases, and transplantation rejection. The findings show that BTLA-neutralizing antibodies can inhibit tumor development (50) , while agonistic anti-BTLA antibody treatment reduces inflammation (63, 95) and prolongs allograft survival (108, 110, 111) . However, these antibodies may not always act exactly as predicted, since different BTLA antibodies may have opposite functions. Confusingly, even the same clone antibody has been reported to exert opposite effects (75, 85, 117) . Furthermore, considering that BTLA/HVEM can deliver bidirectional signals, antibodies targeting BTLA will cause complex biological effects. Although few therapeutic agents targeting inhibitory receptors (such as CTLA-4Ig and anti-PD-1) are being used in clinical trials, the complexity of BTLA signaling system remains a challenge for the development of targeted therapies.

In addition to BTLA, HVEM interacts with LIGHT and CD160. All the four molecules form the HVEM/BTLA/CD160/ LIGHT signaling network. For HVEM, binding to BTLA mediates the inhibitory effect, while binding to LIGHT mediates the activation effect. The role of CD160 remains controversial as it generates activating as well as inhibitory signals. In response to HVEM ligation, CD160 delivers coinhibitory signals to CD4 + T cells (8), whereas it provides costimulatory signals to CD8 + T (118) and NK (119) cells. Additionally, BTLA can provide negative feedback for NK cell activation by competing with CD160 (119). 

Reported functions (references)

Tumors ◾ BTLA expression increases in patients with GBC (44), HCC (45, 46) , DLBCL (47) , and melanoma (48, 49) , and is associated with poor prognosis. Inflammatory diseases ◾ Alleviates allergic airway inflammation (62), contact hypersensitivity (63), colitis (64) , and acute hepatitis (65) in mice.

◾ Increased BTLA correlates with sepsis severity in patients (68) (69) (70) (71) . Therefore, HVEM is a bidirectional switch, and its outcome is determined by the ligand involved. In addition, BTLA/HVEM signaling can antagonize LIGHT/HVEM signaling-mediated effector cell activation (14) and additional studies are needed to elucidate which is the predominant pathway. Furthermore, BTLA/ HVEM signaling is also bidirectional. Although BTLA delivers inhibitory signals, its engagement with HVEM induces HVEMmediated NF-kB activation, which is important for the induction of proinflammatory and cell survival genes (120) . This also suggests the possibility that the pro-survival effect mediated by BTLA/HVEM ligation may be caused by HVEM-NF-kB signaling rather than BTLA signaling. The unique interaction between BTLA and HVEM allows for a system of bidirectional signaling (Figure 1) , which contributes to the understanding of the opposite or dual roles of HVEM and BTLA and the approach for their specific targeting in treatment.

ZN and KL are responsible for preparation of the published work. HX is responsible for supervision, review and editing and funding acquisition. All authors contributed to the article and approved the submitted version. 

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Characterization of phosphotyrosine binding motifs in the cytoplasmic domain of B and T lymphocyte attenuator required for association with protein tyrosine phosphatases SHP-1 and SHP-2

BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1

Extrathymic Regulatory T Cells and Tolerance by Dendritic Cells

BTLA-Expressing Dendritic Cells in Patients With Tuberculosis Exhibit Reduced Production of IL-12/IFN-a and Increased Production of IL-4 and TGF-b, Favoring Th2 and Foxp3(+) Treg Polarization

Immunoregulation of Dendritic Cell Subsets by Inhibitory Receptors in Urothelial Cancer

Clinical significance of tumor-infiltrating immune cells focusing on BTLA and Cbl-b in patients with gallbladder cancer

Distinct Changes of BTLA and HVEM Expressions in Circulating CD4(+) and CD8(+) T Cells in Hepatocellular Carcinoma Patients

BTLA identifies dysfunctional PD-1-expressing CD4(+) T cells in human hepatocellular carcinoma

BTLA marks a less cytotoxic T-cell subset in diffuse large B-cell lymphoma with high expression of checkpoints

BTLA mediates inhibition of human tumor-specific CD8+ T cells that can be partially reversed by vaccination

CD8(+) T cells specific for tumor antigens can be rendered dysfunctional by the tumor microenvironment through upregulation of the inhibitory receptors BTLA and PD-1

Downregulation of BTLA on NKT Cells Promotes Tumor Immune Control in a Mouse Model of Mammary Carcinoma

Distinct expression and inhibitory function of B and T lymphocyte attenuator on human T cells

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Specific lymphocyte subsets predict response to adoptive cell therapy using expanded autologous tumor-infiltrating lymphocytes in metastatic melanoma patients

BTLA marks a less-differentiated tumor-infiltrating lymphocyte subset in melanoma with enhanced survival properties

Multifaceted Role of BTLA in the Control of CD8(+) T-cell Fate after Antigen Encounter

Association of 3' nearby gene BTLA polymorphisms with the risk of renal cell carcinoma in the Polish population

Intragenic Variations in BTLA Gene Influence mRNA Expression of BTLA Gene in Chronic Lymphocytic Leukemia Patients and Confer Susceptibility to Chronic Lymphocytic Leukemia

Investigation of BTLA tagging variants with risk of esophagogastric junction adenocarcinoma

Association of BTLA gene polymorphisms with the risk of malignant breast cancer in Chinese women of Heilongjiang Province

Association between BTLA polymorphisms and susceptibility to esophageal squamous cell carcinoma in the Chinese population

Cutting edge: B and T lymphocyte attenuator and programmed death receptor-1 inhibitory receptors are required for termination of acute allergic airway inflammation

Therapeutic potential of B and T lymphocyte attenuator expressed on CD8+ T cells for contact hypersensitivity

BTLA associates with increased Foxp3 expression in CD4(+) T cells in dextran sulfate sodium-induced colitis

Cutting edge: B and T lymphocyte attenuator signaling on NKT cells inhibits cytokine release and tissue injury in early immune responses

BTLA-HVEM Checkpoint Axis Regulates Hepatic Homeostasis and Inflammation in a ConA-Induced Hepatitis Model in Zebrafish

BTLA expression contributes to septic morbidity and mortality by inducing innate inflammatory cell dysfunction

B and T lymphocyte attenuator expression on CD4+ T-cells associates with sepsis and subsequent infections in ICU patients

Attenuator Expression on Regulatory T-Cells in Patients with Severe Sepsis

Changes in the process of alternative RNA splicing results in soluble B and T lymphocyte attenuator with biological and clinical implications in critical illness

Soluble B and T Lymphocyte Attenuator Correlates to Disease Severity in Sepsis and High Levels Are Associated with an Increased Risk of Mortality

Low B and T lymphocyte attenuator expression on CD4+ T cells in the early stage of sepsis is associated with the severity and mortality of septic patients: a prospective cohort study

T cells from patients with Candida sepsis display a suppressive immunophenotype

Ligation of B and T lymphocyte attenuator prevents the genesis of experimental cerebral malaria

Editorial: Therapeutic potential of targeting BTLA

Enhanced Innate Inflammation Induced by Anti-BTLA Antibody in Dual Insult Model of Hemorrhagic Shock/Sepsis

Rs1982809 is a functional biomarker for the prognosis of severe post-traumatic sepsis and MODs

Regulatory T Cell Dysfunction Acquiesces to BTLA+ Regulatory B Cells Subsequent to Oral Intervention in Experimental Autoimmune Encephalomyelitis

Development of autoimmune hepatitis-like disease and production of autoantibodies to nuclear antigens in mice lacking B and T lymphocyte attenuator

Lymphocytes in Multiple Sclerosis: Bregs and BTLA/CD272 Expressing-CD19+ Lymphocytes Modulate Disease Severity. Sci Rep

BTLA Expression on Th1, Th2 and Th17 Effector T-Cells of Patients with Systemic Lupus Erythematosus Is Associated with Active Disease

Defective BTLA functionality is rescued by restoring lipid metabolism in lupus CD4+ T cells

Lack of B and T lymphocyte attenuator exacerbates autoimmune disorders and induces Fas-independent liver injury in MRL-lpr/lpr mice

Association study between B-and T-lymphocyte attenuator gene and type 1 diabetes mellitus or systemic lupus erythematosus in the Japanese population

BTLA targeting modulates lymphocyte phenotype, function, and numbers and attenuates disease in nonobese diabetic mice

Dendritic cells expressing BTLA induces CD8+ T cell tolerance and attenuates the severity of diabetes

The Expression of BTLA Was Increased and the Expression of HVEM and LIGHT Were Decreased in the T Cells of Patients with Rheumatoid Arthritis

Association of a BTLA gene polymorphism with the risk of rheumatoid arthritis

A functional polymorphism in B and T lymphocyte attenuator is associated with susceptibility to rheumatoid arthritis

Next-Generation Sequencing of T and B Cell Receptor Repertoires from COVID-19 Patients Showed Signatures Associated with Severity of Disease

Expression and clinical significance of B and T lymphocyte attenuator on CD4(+) and CD8 (+) T cells from patients with pulmonary tuberculosis

B and T lymphocyte attenuator is highly expressed on CMV-specific T cells during infection and regulates their function

B and T lymphocyte attenuator is highly expressed on intrahepatic T cells during chronic HBV infection and regulates their function

Hepatic expansion of virusspecific CD8(+)BTLA(+) T cells with regulatory properties in chronic hepatitis B virus infection

Expression of B and T Lymphocyte Attenuator in Patients with Severe Community-Acquired Pneumonia and the Effect of Steroid Therapy in a Mouse Model

Cutting Edge: the BTLA-HVEM regulatory pathway interferes with protective immunity to intestinal Helminth infection

Expression of B and T lymphocyte attenuator (BTLA) in macrophages contributes to the fulminant hepatitis caused by murine hepatitis virus strain-3

B and T lymphocyte attenuator restricts the protective immune response against experimental malaria

B and T lymphocyte attenuator tempers early infection immunity

A BTLA-mediated bait and switch strategy permits Listeria expansion in CD8a(+) DCs to promote long-term T cell responses

BTLA interaction with HVEM expressed on CD8(+) T cells promotes survival and memory generation in response to a bacterial infection

CD8 T cell memory to a viral pathogen requires trans cosignaling between HVEM and BTLA

BTLA exhibits immune memory for ab T cells in patients with active pulmonary tuberculosis

Targeting of B and T lymphocyte associated (BTLA) prevents graftversus-host disease without global immunosuppression

Dichotomous regulation of GVHD through bidirectional functions of the BTLA-HVEM pathway

BTLA suppress acute rejection via regulating TCR downstream signals and cytokines production in kidney transplantation and prolonged allografts survival

Role of B and T Lymphocyte Attenuator in Renal Transplant Recipients with Biopsy-Proven Acute Rejection

An agonistic anti-BTLA mAb (3C10) induced generation of IL-10-dependent regulatory CD4+ T cells and prolongation of murine cardiac allograft

Differential effects of B and T lymphocyte attenuator and programmed death-1 on acceptance of partially versus fully MHC-mismatched cardiac allografts

Combined coinhibitory and costimulatory modulation with anti-BTLA and CTLA4Ig facilitates tolerance in murine islet allografts

Negative and positive co-signaling with anti-BTLA (PJ196) and CTLA4Ig prolongs islet allograft survival

The synergism of B and T lymphocyte attenuator (BTLA) and cytotoxic T lymphocyte associated antigen-4 (CTLA-4) attenuated acute T-cell mediated rejection and prolonged renal graft survival

B-and T-lymphocyte attenuator targeting protects against the acute phase of graft versus host reaction by inhibiting donor anti-host cytotoxicity

Selective blockade of herpesvirus entry mediator-B and T lymphocyte attenuator pathway ameliorates acute graft-versus-host reaction

T follicular helper expansion and humoral-mediated rejection are independent of the HVEM/BTLA pathway

Associations between HVEM/LIGHT/BTLA/CD160 polymorphisms and the occurrence of antibody-mediate rejection in renal transplant recipients

A crucial role for HVEM and BTLA in preventing intestinal inflammation

CD160 Stimulates CD8(+) T Cell Responses and Is Required for Optimal Protective Immunity to Listeria monocytogenes

CD160 activation by herpesvirus entry mediator augments inflammatory cytokine production and cytolytic function by NK cells

Regulation of inflammation, autoimmunity, and infection immunity by HVEM-BTLA signaling

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.Copyright © 2021 Ning, Liu and Xiong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.