High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion

Qu, Yachao; Huang, Yong; Liu, Di; Huang, Yinuo; Zhang, Zhiyi; Mi, Zhiqiang; An, Xiaoping; Tong, Yigang; Lu, Jun

doi:https://doi.org/10.1155/2016/8594107

Canadian Journal of Infectious Diseases and Medical Microbiology

On this page

Abstract Introduction Materials and Methods Results Discussion Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2016 | Article ID 8594107 | https://doi.org/10.1155/2016/8594107

High-Throughput Analysis of the T Cell Receptor Beta Chain Repertoire in PBMCs from Chronic Hepatitis B Patients with HBeAg Seroconversion

Yachao Qu,¹Yong Huang,²Di Liu,³Yinuo Huang,¹Zhiyi Zhang,²Zhiqiang Mi,²Xiaoping An,²Yigang Tong,²and Jun Lu¹

Academic Editor: Roshanak Tolouei Semnani

Received27 Mar 2016

Revised04 Jul 2016

Accepted21 Jul 2016

Published13 Oct 2016

Abstract

T lymphocytes are the most important immune cells that affect both the development and treatment of hepatitis B. We used high-throughput sequencing to determine the diversity in the V and J regions of the TCRβ chain in 4 chronic hepatitis B patients before and after HBeAg seroconversion. Here, we demonstrate that the 4 patients expressed -4 at the highest frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, and was the second most common, with frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. No significant changes were observed following seroconversion. With regard to the Jβ gene, Jβ2-1 was the most commonly expressed in the 4 patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Analysis of the V-J region genes revealed several differences, including significant increases in the expression levels of V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 and a decrease in that of V19-01-J2-3. These results illustrate the presence of biased TCRVβ and Jβ gene expression in the chronic hepatitis B patients. TRBVβ12-4, , Jβ2-1, V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 may be associated with the development and treatment of CHB.

1. Introduction

According to the World Health Organization, two billion people worldwide are infected with hepatitis B virus (HBV), and 350 million people are chronically infected. Approximately one million people die each year due to HBV infection, which leads to cirrhosis, liver failure, and/or hepatocellular carcinoma [1]. Therefore, understanding the pathogenesis of chronic hepatitis B (CHB) is of great importance. The natural history of HBV is influenced by the host, virus, and microenvironment [2]. Circumstantial evidence suggests that HBV does not directly lead to hepatocyte necrosis. Hepatocyte injury caused by HBV is believed to be mediated by the cellular immune response against the virus [3]. This response is relatively strong in acute, self-limited HBV infection. However, circulating HBV-specific T cells are rarely detected in CHB [4].

A healthy adult has approximately different polyclonal T cells, each of which expresses a particular T cell receptor (TCR) [5]. TCR is a heterodimer consisting of α and β protein chains that determine T lymphocyte specificity [6]. TCR diversity is generated by the somatic recombination of the V, D (for TCRβ only), and J gene segments [7]. In the process of T cell maturation, allelic exclusion ensures that only one β chain protein is expressed in T cells [8]. Therefore, TCRβ chains can be used as molecular fingerprints to identify T cell clones. Human TCRβ includes 48 different functional V, 13 J, and 2 D gene segments in addition to 1 J and 18 V pseudogenes, which can be rearranged [9]. A number of techniques have been applied to analyze the TCR repertoire [10]; for example, flow cytometry is commonly employed; however, this method is limited by anti-TRB antibody specificity [11]. Gene melting spectral pattern (GMSP) assay, which is used to analyze the TCR gene family, is widely used [12]. Because this technique requires a large number of PCR reactions including primers for all possible V and J genes, its application is limited. Delayed data availability and the inability to detect variations in TCRβ chain sequences are further drawbacks. More powerful diagnostic tools are therefore needed to accurately assess TCR diversity that can be used to monitor immune reconstitution, therapeutic responses, and disease status and to identify the T cell clonotypes in different diseases.

In recent years, next-generation sequencing (NGS), a fast and accurate new method, has been applied in various fields of medicine, with high coverage and massively parallel DNA sequence identification [13, 14]. In this study, we collected peripheral blood mononuclear cells (PBMCs) from CHB patients undergoing treatment. Using NGS, we compared the TCRβ repertoire before and after HBeAg seroconversion in these patients and determined the pathogenesis of CHB during treatment. This study has generated new ideas for the development of effective individual treatment strategies and research technology platforms.

The purpose of our study was to elucidate the molecular portrait of TCRβ chains in PBMCs from CHB patients and to reveal the role of cell-mediated immunity in the pathogenesis of chronic HBV infection to facilitate the development of individualized treatment.

2. Materials and Methods

2.1. Subjects

Between April 2012 and July 2013, 18 patients with hepatitis B surface antigen (HBsAg) that tested positive for at least 6 months were enrolled in our study. The subjects were selected at the Beijing You’an Hospital, affiliated with Capital Medical University. Individuals with hepatitis C or D or human immunodeficiency (HIV) virus or autoimmune disease and other malignancies were excluded. This study was performed in accordance with the principles of the Declaration of Helsinki. All patients provided informed consent before the initiation of the study. Each patient was treated orally with 0.5 mg entecavir (Bristol-Myers Squibb, USA) once a day for 48 weeks and injection of 1.6 mg thymosin α1 (Patheon Italia SPA, Italy) every other day for 24 weeks. Every three months, the patients visited the outpatient department for examination.

2.2. Serological and Biochemical Assays

ALT and TBIL levels were measured with an automatic biochemical analyzer (Beckman 5400, California, USA), and HBV DNA was quantified using real-time fluorescence quantitative PCR (Applied Biosystems 5700, California, USA) according to the manufacturer’s protocol. HBsAg, HBsAb, HBeAg, anti-Hbe, and anti-HBc levels were assessed by enzyme immunoassays (Roche E601, Basel, Switzerland).

2.3. Isolation and Cryopreservation of PBMCs

PBMCs were prepared from 2 mL of whole blood collected from CHB patients by Lymphoprep (Axis-Shield, Oslo, Norway). Approximately PBMCs can be obtained with this method. Cells were mixed into 1 mL RPMI 1640 medium (Life, New York, USA), which contains 10% MDSO and 20% bovine serum, and then placed in a Cryo 1° Freezing Container (Nalgene, USA) for storage at −80° until use in the experiments.

2.4. Total RNA Isolation and cDNA Synthesis

Total RNA was extracted from PBMCs using RNA (RNeasy kit) according to the manufacturer’s instructions, and cDNA synthesis was performed immediately with cDNA (Superscript II).

2.5. PCR cDNA Amplification and TCR Chain Sequencing

PCR was performed with a Thermal Cycler PCR System 2720 (Gene Company Limited). One round of PCR was carried out to amplify cDNA. Each 50 μL PCR reaction contained 2 μL cDNA, 12 μL dd, 25 μL Premix Ex Taq (TaKaRa), 200 nM of the specific primer CP1 (GCACCTCCTTCCCATTCAC, which targets C region genes [15]), and 2 μM of the degenerate primer VP1 (GCIITKTIYTGGTAYMGACA, which targets the V region and covers 42 Vβ chains [15]). The PCR program was as follows: one cycle at 94° for 10 min, followed by 40 cycles at 94° for 30 s, 50° for 30 s, and 72° for 30 s, with a final 10 min extension at 72° and a 4° hold. Ten milliliters of each PCR product was run on a 2% agarose gel (150 V, 45 min), and products of approximately 400 bp were excised and purified using a Gel Extraction Kit (Qiagen, Hilden, Germany). The library was prepared according to the Ion Torrent sequencing manufacturer’s instructions. The PGM sensed the H+ signal as sequencing-by-synthesis progressed [16].

2.6. Analysis of TCR Diversity

A Blast+ [17] search was carried out for the alignment-based identification of individual amplicons against TCRβ chain germ line genes (63 TRBV, 2 TRBD, and 14 TRBJ), which were derived from IMGT/GENE-DB database (http://imgt.cines.org/). A homemade Perl script was used to analyze the Blast results and quantify the TRBV and TRBJ gene pairings, including the TRBV-only and TRBJ-only amplicons.

3. Results

3.1. Clinical Outcomes

After antiviral treatment with entecavir and thymosin α1 for 48 weeks, 98% (17/18) of the patients had no detectable serum HBV DNA, the serum ALT level returned to normal, and 22.2% (4/18) of the patients achieved HBeAg seroconversion. No patient had undergone HBsAg seroconversion by week 48 of treatment. PBMCs were collected from the 4 patients before and after HBeAg seroconversion for TCR sequencing, and their clinical characteristics are summarized in Table 1.

Sequencing Data. The total numbers of sequencing reads for the 4 paired samples ranged from 370,210 to 685,596, with an average length of approximately 230 bp (Table 2). The average length may have been smaller than the library length because the PGM prevented some of the PCR amplicons from being fully sequenced. The ratio of Q20 (quality score of ≥20) bases to total bases sequenced ranged from 83.2% to 86.2%, indicating a high level of sequencing quality.

3.2. Biased Vβ and Jβ Gene Segments within TCRs

Among the productively rearranged clones from the PBMCs of the patients, 30 Vβ gene segments and 14 Jβ gene segments were identified. The serial results of relative TCRVβ and Jβ expression in the four patients (P1–P4) before and after HBeAg seroconversion are shown in Figure 1.

(a)

(b)

The gene fragments, which initially accounted for more than 5%, were defined as the advantage segments. The expression levels of the Vβ genes were diverse. Vβ12-4 was the most common segment detected in the PBMCs of the four patients, with frequencies of 10.6%, 9.2%, 17.5%, and 7.5%, respectively. Vβ28 was also frequently found in the four patients at frequencies of 7.8%, 6.7%, 5.3%, and 10.9%, respectively. Vβ12-5 (10.6%, 9.1%, and 5.3%), Vβ19 (12.3%, 10.6%, and 5.9%), and Vβ7-2 (6.5%, 5.6%, and 9.8%) were frequently observed in three of the patients, while other gene segments were detected in less than 5% of the patients. Furthermore, we analyzed the differences between the two periods (before and after HBeAg seroconversion). A greater than 3% fluctuation in the relative TCRVβ gene expression ratio between the two stages was defined as a significant change. Several TCRVβ families showed changes between the two time periods (P1: Vβ12-4 was upregulated and Vβ12-5, Vβ19, and Vβ28 were downregulated; P2: Vβ12-5, Vβ19, and Vβ28 were downregulated; P3: Vβ10-3 and Vβ19 were upregulated and Vβ12-4 and Vβ23-1 were downregulated; and P4: Vβ28 was upregulated and Vβ27 was downregulated). However, no common highly fluctuating TCRVβ segment was found in the patients. Moreover, there was no correlation between the changes in TCRVβ gene expression and the serum ALT or TBIL level.

With regard to Jβ gene expression, Jβ2-1 was the most abundant segment in the PBMCs of the four patients at frequencies of 5.8%, 6.5%, 11.3%, and 7.3%, respectively. Jβ2-3 (6.4% and 17.3%) and Jβ2-7 (8.8% and 5.8%) were frequently expressed in two of the patients, while other gene segments were detected in less than 5% of cells from most of the patients. We also analyzed the changes in TCRJβ gene expression between the two periods. There were no significant differences between the two stages for the first two patients (P1 and P2). However, several Jβ segments were upregulated in the third patient (P3) (Jβ1-1, Jβ1-2, Jβ1-5, Jβ2-1, Jβ2-3, Jβ2-5, and Jβ2-7), and Jβ2-1 was upregulated, while Jβ2-3 was downregulated, in the fourth patient (P4). Given that the third patient (P3) was the only female of the four subjects, it is possible that TCRJβ expression is affected by gender, further influencing the efficacy of therapy. Similarly, there was no correlation between the changes in TCRJβ gene expression and the serum ALT or TBIL level.

3.3. Restricted Changes in TCRβV-J Gene Pairing in the Four Patients

The sequencing reads showing similarity to certain V and J genes were defined as TCRβV_J gene pairings. TCRβV_J gene pairings were detected in the raw reads of four patients separately (both before and after treatment). Differences in the expression of each combination detected in the four patients are shown in Figure 2. Among the patients, there were several combinations that tended to be similarly differentially expressed following the shift from HBeAg positive to negative. For example, the combinations V7-2-01-J2-1, V12-4-J1-1, and V28-1-J1-5 were upregulated and V19-01-J2-3 was downregulated significantly following seroconversion.

4. Discussion

HBV infection is a major public health concern because it has significant impacts on human health. The different outcomes of HBV infection are determined by the immune status of the host. In acute self-limited HBV infection, the T cell response is strong, while it is relatively weak in patients with CHB [18]. Moreover, Dou et al. [19] have demonstrated that the population of HBcAg-activated T cells is altered during the course of CHB. The TCRβ chain can reflect the status and role of T cells. There are also three complementarity-determining regions (CDR1, CDR2, and CDR3) in the TCR. Molecular structural analysis has revealed that CDR3 mainly recognizes MHC molecules bound to antigenic peptides [20, 21]. Hence, analysis of CDR3 can reveal changes in antigen-stimulated T cells [22, 23], the number of T cell clones, and T cell functioning [24, 25].

Analysis of TCR usage in patients can aid in the understanding of immune responses under a number of conditions during the course of a disease [26]. Sugyo et al. [27] monitored the TCRβ chains of 4 healthy controls from 4 to 8 weeks, revealing that there was no significant change in the ratio. Many studies have confirmed that, in patients with viral infection or cancer, the frequency of antigen-specific TCRs differs [28, 29]. In our study, we observed several patients with the increased and/or decreased expression of TCR families, which is consistent with previous studies suggesting that the T cell response to HBV employs diverse TCR families [12, 30]. The findings of this study are also in agreement with those of prior studies demonstrating that TCR families are biased [31]. These observations may be correlated with the different epitopes of HBV or to the different HLA phenotypes [31, 32].

Most patients with CHB are successfully treated with antiviral drugs. However, some require long-term therapy, and relapse is common. At present, HBV therapy is primarily based on the uses of nucleoside analogs and immunomodulating agents. The effects of these treatments are closely correlated with the rescue of T cell function, especially among HBV-specific T cells [4]. Furthermore, these treatments are often limited by drug resistance and side effects. Moreover, the response rate is low, and many patients subsequently relapse [33]. Hence, it is necessary to develop new interventions for HBV infection.

In recent years, many researchers have modified T cells with specific TCR genes to cure cancer and other diseases. Morgan et al. [34] have demonstrated that TCR gene-modified T cells could be used for treating melanoma. Xue et al. [35] engineered patients’ T cells to express WT1-TCR, which eliminates autologous leukemia progenitor cells, in an in vivo model. Their findings provide a strong basis for the planned WT1-TCR gene therapy trials of leukemia patients. Gehring et al. [36] used vector-mediated gene transfer to introduce HLA A2-restricted, HBV-specific TCRs into T cells of chronic HBV and HBV-related HCC patients and found that these genetically modified T cells could be used to reconstitute virus-specific T cell immunity in the chronic HBV patients and target tumors in the HBV-related HCC patients. In 2013, Koh et al. [37] performed electroporation of mRNA-encoding anti-HBV TCRs to explore a safer and more practical method for cell therapy of HCC that may also be employed to treat other HBV-related diseases. Krebs et al. [38] have demonstrated that T cells with a chimeric antigen receptor (CAR) specific for HBV envelope proteins localized to the livers of mice to reduce HBV replication cause only temporary damage. This immune therapy could be developed for CHB patients, regardless of their HLA type. Similar studies have also been conducted on acute hepatitis B and chronic severe hepatitis B patients [39, 40].

NGS was carried out to analyze TCR expression before and after HBeAg seroconversion in patients with CHB. High-throughput sequencing has been used to monitor the drug resistance of HBV [41]. Recently, Robins et al. [42] have studied TCR diversity in 2 healthy adults based on NGS and spectratyping, similarly showing the improved sensitivity of the former. Han et al. [43] have used high-throughput sequencing and suggested that comparison of the T cell repertoires of tissue and blood could be used to distinguish liver cancer patients from healthy adults and from hepatitis patients. Moreover, recent study of Huang et al. [44] has demonstrated that the genomic rearrangement of the V and J segments of TCRβ chain V area may be associated with the chronic progression of HBV and impact on treatment efficacy. We used this method to determine the exact length and sequence of CDR3 to identify TCRVβ and Jβ genes.

A comparison of the two regions indicated that the TCRβ families Vβ12-4, Vβ12-5, Vβ19, Vβ28, Vβ7-2, Jβ2-1, Jβ2-3, and Jβ2-7 were more frequently expressed in the HBeAg-positive patients than the other TCR family members. These results are consistent with those of other studies suggesting that TCRVβ7 and Vβ12 are more abundant than other TCRVβ genes in HBV-related infections [19, 40, 45] and other diseases [46].

Moreover, many Vβ-Jβ gene segment combinations were found to change with HBeAg status, and this activity may be specific to HBV antigens. However, it was difficult to identify the HBV peptides that these TCRs reacted to. Such biased usage of TCRs has also been reported by studies of multiple sclerosis, primary biliary cirrhosis, and autoimmune hepatitis [47–51]. Still, the identification of TCR families can help to elucidate the pathogenesis of and improve the treatment of hepatitis B.

In conclusion, the characteristics of TCRs in CHB patients are biased and involve multiple TCRβ families. The TCRβV7-2-01-J2-1, V12-4-J1-1, V28-1-J1-5, and V19-01-J2-3 genes may contribute more to the emergence and maintenance of anti-HBe in CHB patients and may represent potential targets for a therapeutic vaccine for CHB. Crystal structure studies are needed in the future.

Competing Interests

The authors who took part in this study declare that they have nothing to disclose regarding funding or competing interests with respect to this manuscript.

Authors’ Contributions

Di Liu, Yigang Tong, and Jun Lu conceived and designed the experiments. Yachao Qu, Yong Huang, and Xiaoping An performed the experiments. Yong Huang, Zhiyi Zhang, Zhiqiang Mi, and Yachao Qu analyzed the data. Yachao Qu, Yong Huang, and Di Liu wrote the paper. Yachao Qu and Yong Huang contributed equally to this work.

Acknowledgments

The authors thank Xuli Bao and Lei Zhang for collecting samples. This study was supported by the “215” high-level health technology project (2011) and the “12th Five-Year” plan of major science and technology projects for major infectious disease prevention and control (2014ZX10002002-001-002).

Supplementary Materials

We have also do some research on T cell functional assays. Compared with the baseline, the percentage of Cytotoxic T lymphocytes(CTL) has been increased after HBeAg seroconversion which demonstrated the CTL play an important role in the treatment of HBV. The results of percentage of CTL in the patient 2 and 3 before and after HBeAg seroconversion are shown in Supplement data.

Supplementary Material

References

World Health Organization, “Hepatitis B,” Fact Sheet 204, WHO, Geneva‎, Switzerland, 2012.
View at: Google Scholar
H. J. Yim and A. S.-F. Lok, “Natural history of chronic hepatitis B virus infection: what we knew in 1981 and what we know in 2005,” Hepatology, vol. 43, no. 2, pp. S173–S181, 2006.
View at: Publisher Site | Google Scholar
D. R. Milich, “Immune response to hepatitis B virus proteins: relevance of the murine model,” Seminars in Liver Disease, vol. 11, no. 2, pp. 93–112, 1991.
View at: Publisher Site | Google Scholar
C. Boni, A. Penna, A. Bertoletti et al., “Transient restoration of anti-viral T cell responses induced by lamivudine therapy in chronic hepatitis B,” Journal of Hepatology, vol. 39, no. 4, pp. 595–605, 2003.
View at: Publisher Site | Google Scholar
T. P. Arstila, A. Casrouge, V. Baron, J. Even, J. Kanellopoulos, and P. Kourilsky, “A direct estimate of the human αβ T cell receptor diversity,” Science, vol. 286, no. 5441, pp. 958–961, 1999.
View at: Publisher Site | Google Scholar
K. C. Garcia, L. Teyton, and I. A. Wilson, “Structural basis of T cell recognition,” Annual Review of Immunology, vol. 17, pp. 369–397, 1999.
View at: Publisher Site | Google Scholar
M. Kronenberg, G. Siu, L. E. Hood, and N. Shastri, “The molecular genetics of the T-cell antigen receptor and T-cell antigen recognition,” Annual Review of Immunology, vol. 4, pp. 529–591, 1986.
View at: Publisher Site | Google Scholar
B. L. Brady, N. C. Steinel, and C. H. Bassing, “Antigen receptor allelic exclusion: an update and reappraisal,” The Journal of Immunology, vol. 185, no. 7, pp. 3801–3808, 2010.
View at: Publisher Site | Google Scholar
M.-P. Lefranc, “IMGT, the international ImMunoGeneTics database®,” Nucleic Acids Research, vol. 31, no. 1, pp. 307–310, 2003.
View at: Publisher Site | Google Scholar
J. Even, A. Lim, I. Puisieux et al., “T-cell repertoires in healthy and diseased human tissues analysed by T-cell receptor β-chain CDR3 size determination: evidence for oligoclonal expansions in tumours and inflammatory diseases,” Research in Immunology, vol. 146, no. 2, pp. 65–80, 1995.
View at: Publisher Site | Google Scholar
J. P. Maciejewski, C. O'Keefe, L. Gondek, and R. Tiu, “Immune-mediated bone marrow failure syndromes of progenitor and stem cells: molecular analysis of cytotoxic T cell clones,” Folia Histochemica et Cytobiologica, vol. 45, no. 1, pp. 5–14, 2007.
View at: Google Scholar
J. Yang, J. Chen, J. He et al., “Profiling the repertoire of T-cell receptor beta-chain variable genes in peripheral blood lymphocytes from subjects who have recovered from acute hepatitis B virus infection,” Cellular and Molecular Immunology, vol. 11, no. 4, pp. 332–342, 2014.
View at: Publisher Site | Google Scholar
R. A. Bull, F. Luciani, K. McElroy et al., “Sequential bottlenecks drive viral evolution in early acute hepatitis C virus infection,” PLoS Pathogens, vol. 7, no. 9, Article ID e1002243, 2011.
View at: Publisher Site | Google Scholar
F. Di Giallonardo, O. Zagordi, Y. Duport et al., “Next-generation sequencing of HIV-1 RNA genomes: determination of error rates and minimizing artificial recombination,” PLoS ONE, vol. 8, no. 9, Article ID e74249, 2013.
View at: Publisher Site | Google Scholar
D. Zhou, R. Srivastava, V. Grummel, S. Cepok, H.-P. Hartung, and B. Hemmer, “High throughput analysis of TCR-β rearrangement and gene expression in single T cells,” Laboratory Investigation, vol. 86, no. 3, pp. 314–321, 2006.
View at: Publisher Site | Google Scholar
E. Pennisi, “Semiconductors inspire new sequencing technologies,” Science, vol. 327, no. 5970, p. 1190, 2010.
View at: Publisher Site | Google Scholar
C. Camacho, G. Coulouris, V. Avagyan et al., “BLAST+: architecture and applications,” BMC Bioinformatics, vol. 10, article 421, 2009.
View at: Publisher Site | Google Scholar
E. Sandalova, D. Laccabue, C. Boni et al., “Increased levels of arginase in patients with acute hepatitis B suppress antiviral T cells,” Gastroenterology, vol. 143, no. 1, pp. 78–87.e3, 2012.
View at: Publisher Site | Google Scholar
H.-Y. Dou, J.-C. Wu, W.-L. Peng et al., “Analysis of T cell receptor V(β) gene usage during the course of disease in patients with chronic hepatitis B,” Journal of Biomedical Science, vol. 5, no. 6, pp. 428–434, 1998.
View at: Google Scholar
P. Marrack and J. Kappler, “Positive selection of thymocytes bearing αβ T cell receptors,” Current Opinion in Immunology, vol. 9, no. 2, pp. 250–255, 1997.
View at: Publisher Site | Google Scholar
P. Miqueu, M. Guillet, N. Degauque, J.-C. Doré, J.-P. Soulillou, and S. Brouard, “Statistical analysis of CDR3 length distributions for the assessment of T and B cell repertoire biases,” Molecular Immunology, vol. 44, no. 6, pp. 1057–1064, 2007.
View at: Publisher Site | Google Scholar
J.-W. Du, J.-Y. Gu, J. Liu et al., “TCR spectratyping revealed T lymphocytes associated with graft-versus-host disease after allogeneic hematopoietic stem cell transplantation,” Leukemia and Lymphoma, vol. 48, no. 8, pp. 1618–1627, 2007.
View at: Publisher Site | Google Scholar
M. Okajima, T. Wada, M. Nishida et al., “Analysis of T cell receptor Vβ diversity in peripheral CD4⁺ and CD8⁺ T lymphocytes in patients with autoimmune thyroid diseases,” Clinical and Experimental Immunology, vol. 155, no. 2, pp. 166–172, 2009.
View at: Publisher Site | Google Scholar
A. Leimgruber, M. Ferber, M. Irving et al., “Tcrep 3D: an automated in silico approach to study the structural properties of tcr repertoires,” PLoS ONE, vol. 6, article e26301, 2011.
View at: Publisher Site | Google Scholar
D. K. Sethi, D. A. Schubert, A.-K. Anders et al., “A highly tilted binding mode by a self-reactive T cell receptor results in altered engagement of peptide and MHC,” The Journal of Experimental Medicine, vol. 208, no. 1, pp. 91–102, 2011.
View at: Publisher Site | Google Scholar
K. S. Seo, J. Y. Park, D. S. Terman, and G. A. Bohach, “A quantitative real time PCR method to analyze T cell receptor Vβ subgroup expansion by staphylococcal superantigens,” Journal of Translational Medicine, vol. 8, article 2, 2010.
View at: Publisher Site | Google Scholar
S. Sugyo, K. Yuh, K. Nakamura et al., “An analysis of T cell antigen receptor variable β genes during the clinical course of patients with chronic hepatitis B,” Journal of Gastroenterology and Hepatology, vol. 14, no. 4, pp. 333–338, 1999.
View at: Publisher Site | Google Scholar
J. J. Miles, D. C. Douek, and D. A. Price, “Bias in the αΒ T-cell repertoire: implications for disease pathogenesis and vaccination,” Immunology and Cell Biology, vol. 89, no. 3, pp. 375–387, 2011.
View at: Publisher Site | Google Scholar
N. J. Singh, J. K. Bando, and R. H. Schwartz, “Subsets of nonclonal neighboring CD4⁺ T cells specifically regulate the frequency of individual antigen-reactive T cells,” Immunity, vol. 37, no. 4, pp. 735–746, 2012.
View at: Publisher Site | Google Scholar
C.-F. Huang, S.-S. Lin, Y.-C. Ho, F.-L. Chen, and C.-C. Yang, “The immune response induced by hepatitis B virus principal antigens,” Cellular & Molecular Immunology, vol. 3, no. 2, pp. 97–106, 2006.
View at: Google Scholar
X.-S. Yao, G.-W. Zhang, L. Ma et al., “Analysis of the CDR3 length of TCR αβ T cells in the peripheral blood of patients with chronic hepatitis B,” Hepatology Research, vol. 35, no. 1, pp. 10–18, 2006.
View at: Publisher Site | Google Scholar
C. P. Desmond, A. Bartholomeusz, S. Gaudieri, P. A. Revill, and S. R. Lewin, “A systematic review of T-cell epitopes in hepatitis B virus: identification, genotypic variation and relevance to antiviral therapeutics,” Antiviral Therapy, vol. 13, no. 2, pp. 161–175, 2008.
View at: Google Scholar
M. G. Ghany and E. C. Doo, “Management of chronic hepatitis B,” Gastroenterology Clinics of North America, vol. 33, no. 3, pp. 563–579, 2004.
View at: Publisher Site | Google Scholar
R. A. Morgan, M. E. Dudley, J. R. Wunderlich et al., “Cancer regression in patients after transfer of genetically engineered lymphocytes,” Science, vol. 314, no. 5796, pp. 126–129, 2006.
View at: Publisher Site | Google Scholar
S.-A. Xue, L. Gao, S. Thomas et al., “Development of a Wilms' tumor antigen-specific T-cell receptor for clinical trials: engineered patient's T cells can eliminate autologous leukemia blasts in NOD/SCID mice,” Haematologica, vol. 95, no. 1, pp. 126–134, 2010.
View at: Publisher Site | Google Scholar
A. J. Gehring, S.-A. Xue, Z. Z. Ho et al., “Engineering virus-specific T cells that target HBV infected hepatocytes and hepatocellular carcinoma cell lines,” Journal of Hepatology, vol. 55, no. 1, pp. 103–110, 2011.
View at: Publisher Site | Google Scholar
S. Koh, N. Shimasaki, R. Suwanarusk et al., “A practical approach to immunotherapy of hepatocellular carcinoma using T cells redirected against hepatitis B virus,” Molecular Therapy—Nucleic Acids, vol. 2, article e114, 2013.
View at: Publisher Site | Google Scholar
K. Krebs, N. Böttinger, L.-R. Huang et al., “T cells expressing a chimeric antigen receptor that binds hepatitis B virus envelope proteins control virus replication in mice,” Gastroenterology, vol. 145, no. 2, pp. 456–465, 2013.
View at: Publisher Site | Google Scholar
J. Wu, L. Wang, Y. Liu et al., “Transgenic expression of T cell receptors on HBV-specific cytotoxic T lymphocytes,” Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, vol. 29, no. 5, pp. 453–457, 2013.
View at: Google Scholar
J. Yang, J. He, H. Lu et al., “Molecular features of the complementarity determining region 3 motif of the T cell population and subsets in the blood of patients with chronic severe hepatitis B,” Journal of Translational Medicine, vol. 9, no. 1, article 210, 2011.
View at: Publisher Site | Google Scholar
M. Rybicka, P. Stalke, M. Dreczewski, T. Smiatacz, and K. P. Bielawski, “High-throughput matrix-assisted laser desorption ionization-time of flight mass spectrometry as an alternative approach to monitoring drug resistance of hepatitis B virus,” Journal of Clinical Microbiology, vol. 52, no. 1, pp. 9–14, 2014.
View at: Publisher Site | Google Scholar
H. S. Robins, P. V. Campregher, S. K. Srivastava et al., “Comprehensive assessment of T-cell receptor β-chain diversity in αβ T cells,” Blood, vol. 114, no. 19, pp. 4099–4107, 2009.
View at: Publisher Site | Google Scholar
Y. Han, X. Liu, Y. Wang et al., “Identification of characteristic TRB V usage in HBV-associated HCC by using differential expression profiling analysis,” OncoImmunology, vol. 4, no. 8, article e1021537, 2015.
View at: Publisher Site | Google Scholar
Y. Huang, H. Ma, S. Wei et al., “nalysis of the complementarity determining regions β-chain genomic rearrangement using high-throughput sequencing in periphery cytotoxic T lymphocytes of patients with chronic hepatitis B,” Molecular Medicine Reports, vol. 14, no. 1, pp. 762–768, 2016.
View at: Publisher Site | Google Scholar
J. Yang, J. Chen, H. Mao et al., “Skewed T-cell receptor beta chain variable gene (TCRBV) usage among different clinical types of patients with chronic HBV infection,” FEMS Immunology and Medical Microbiology, vol. 65, no. 3, pp. 448–455, 2012.
View at: Publisher Site | Google Scholar
S.-W. Qiao, A. Christophersen, K. E. A. Lundin, and L. M. Sollid, “Biased usage and preferred pairing of α-and β-chains of TCRs specific for an immunodominant gluten epitope in coeliac disease,” International Immunology, vol. 26, no. 1, pp. 13–19, 2014.
View at: Publisher Site | Google Scholar
J. R. Oksenberg, S. Stuart, A. B. Begovich et al., “Limited heterogeneity of rearranged T-cell receptor V alpha transcripts in brains of multiple sclerosis patients,” Nature, vol. 353, no. 6339, article 94, 1991.
View at: Google Scholar
M. Arenz, K.-H. Meyer Zum Büschenfelde, and H. F. Löhr, “Limited T cell receptor Vβ-chain repertoire of liver-infiltrating T cells in autoimmune hepatitis,” Journal of Hepatology, vol. 28, no. 1, pp. 70–77, 1998.
View at: Publisher Site | Google Scholar
M. Arenz, S. Pingel, P. Schirmacher, K.-H. Meyer zum Büschenfelde, and H. F. Löhr, “T cell receptor Vβ chain restriction and preferred CDR3 motifs of liver-kidney microsomal antigen (LKM-1)-reactive T cells from autoimmune hepatitis patients,” Liver, vol. 21, no. 1, pp. 18–25, 2001.
View at: Publisher Site | Google Scholar
Y. Hoshino, N. Enomoto, N. Izumi, M. Kurosaki, F. Marumo, and C. Sato, “Limited usage of T-cell receptor β chains and sequences of the complementarity determining region 3 of lymphocytes infiltrating in the liver of autoimmune hepatitis,” Hepatology, vol. 22, no. 1, pp. 142–147, 1995.
View at: Publisher Site | Google Scholar
U. Moebius, M. Manns, G. Hess, G. Kober, K.-H. Meyer Zum Büschenfelde, and S. C. Meuer, “T cell receptor gene rearrangements of T lymphocytes infiltrating the liver in chronic active hepatitis B and primary biliary cirrhosis (PBC): oligoclonality of PBC-derived T cell clones,” European Journal of Immunology, vol. 20, no. 4, pp. 889–896, 1990.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2016 Yachao Qu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

2055

Downloads

1303

Citations