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Published in: BMC Nephrology 1/2017

Open Access 01-12-2017 | Research article

VDJ gene usage among B-cell receptors in ABO-incompatible kidney transplantation determined by RNA-seq Transcriptomic analysis

Authors: Hee Jung Jeon, Kwangsoo Kim, Jae-Ghi Lee, Joon Young Jang, Seongmin Choi, Taishi Fang, Ji-Jing Yan, Miyeun Han, Jong Cheol Jeong, Kyoung-Bun Lee, Tae Jin Kim, Curie Ahn, Jaeseok Yang

Published in: BMC Nephrology | Issue 1/2017

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Abstract

Background

Studies on B-cell subtypes and V(D)J gene usage of B-cell receptors in kidney transplants are scarce. This study aimed to investigate V(D)J gene segment usage in ABO-incompatible (ABOi) kidney transplant (KT) patients compared to that in ABO-compatible (ABOc) KT patients.

Methods

We selected 16 ABOi KT patients with accommodation (ABOiA), 6 ABOc stable KT patients (ABOcS), and 6 ABOi KT patients with biopsy-proven acute antibody-mediated rejection (ABOiR) at day 10, whose graft tissue samples had been stored in the biorepository between 2010 and 2014. Complete transcriptomes of graft tissues were sequenced and analyzed through RNA sequencing (RNA-seq). The international ImMunoGeneTics information system (IMGT®) was used for in-depth comparison of V(D)J gene segment usage.

Results

The mean age of the 28 KT recipients was 43.3 ± 12.8 years, and 53.6% were male. By family, IGHV3, IGHJ4, IGLV2, and IGLJ3 gene segments were most frequently used in all groups, and their usage was not statistically different among the three patient groups. While IGKV3 was most frequently used in both the ABOiA and ABOiR groups, IGKV1 was most commonly used in the ABOcS group. In addition, while IGKJ1 was most commonly used in the ABOiA and ABOcS groups, IGKJ4 was most frequently used in the ABOiR group. According to individual gene segments, IGHV4–34 and IGHV4–30-2 were more commonly used in the ABOiR group than in the ABOiA group, and IGHV6–1 was more commonly used in the ABOcS group than in the ABOiR group. IGLV7–43 was more commonly used in the ABOcS group than in the ABOi group. However, technical variability, small sample size, and potential confounding effects of Rituximab or HLA mismatching are limitations of our study.

Conclusions

Our findings suggest that RNA-seq transcriptomic analyses can provide information on the V(D)J gene usage of B-cell receptors and the mechanisms of accommodation and immune reaction in ABOi KT.
Literature
1.
go back to reference Cecka JM. The OPTN/UNOS Renal Transplant Registry. Clin Transpl. 2005;1–16. Cecka JM. The OPTN/UNOS Renal Transplant Registry. Clin Transpl. 2005;1–16.
2.
go back to reference Tanabe K, Takahashi K, Sonda K, Tokumoto T, Ishikawa N, Kawai T, et al. Long-term results of ABO-incompatible living kidney transplantation: a single-center experience. Transplantation. 1998;65:224–8.CrossRefPubMed Tanabe K, Takahashi K, Sonda K, Tokumoto T, Ishikawa N, Kawai T, et al. Long-term results of ABO-incompatible living kidney transplantation: a single-center experience. Transplantation. 1998;65:224–8.CrossRefPubMed
3.
go back to reference Zschiedrich S, Kramer-Zucker A, Janigen B, Seidl M, Emmerich F, Pisarski P, et al. An update on ABO-incompatible kidney transplantation. Transpl Int. 2015;28:387–97.CrossRefPubMed Zschiedrich S, Kramer-Zucker A, Janigen B, Seidl M, Emmerich F, Pisarski P, et al. An update on ABO-incompatible kidney transplantation. Transpl Int. 2015;28:387–97.CrossRefPubMed
4.
go back to reference Shimmura H, Tanabe K, Ishikawa N, Tokumoto T, Takahashi K, Toma H. Role of anti-a/B antibody titers in results of ABO-incompatible kidney transplantation. Transplantation. 2000;70:1331–5.CrossRefPubMed Shimmura H, Tanabe K, Ishikawa N, Tokumoto T, Takahashi K, Toma H. Role of anti-a/B antibody titers in results of ABO-incompatible kidney transplantation. Transplantation. 2000;70:1331–5.CrossRefPubMed
5.
go back to reference Chopek MW, Simmons RL, Platt JL. ABO-incompatible kidney transplantation: initial immunopathologic evaluation. Transplant Proc. 1987;19:4553–7.PubMed Chopek MW, Simmons RL, Platt JL. ABO-incompatible kidney transplantation: initial immunopathologic evaluation. Transplant Proc. 1987;19:4553–7.PubMed
6.
go back to reference Riley SC, Froscher BG, Linton PJ, Zharhary D, Marcu K, Klinman NR. Altered VH gene segment utilization in the response to phosphorylcholine by aged mice. J Immunol. 1989;143:3798–805.PubMed Riley SC, Froscher BG, Linton PJ, Zharhary D, Marcu K, Klinman NR. Altered VH gene segment utilization in the response to phosphorylcholine by aged mice. J Immunol. 1989;143:3798–805.PubMed
7.
go back to reference Nicoletti C, Borghesi-Nicoletti C, Yang XH, Schulze DH, Cerny J. Repertoire diversity of antibody response to bacterial antigens in aged mice. II. Phosphorylcholine-antibody in young and aged mice differ in both VH/VL gene repertoire and in specificity. J Immunol. 1991;147:2750–5.PubMed Nicoletti C, Borghesi-Nicoletti C, Yang XH, Schulze DH, Cerny J. Repertoire diversity of antibody response to bacterial antigens in aged mice. II. Phosphorylcholine-antibody in young and aged mice differ in both VH/VL gene repertoire and in specificity. J Immunol. 1991;147:2750–5.PubMed
8.
go back to reference Tallmadge RL, Tseng CT, Felippe MJ. Diversity of immunoglobulin lambda light chain gene usage over developmental stages in the horse. Dev Comp Immunol. 2014;46:171–9.CrossRefPubMedPubMedCentral Tallmadge RL, Tseng CT, Felippe MJ. Diversity of immunoglobulin lambda light chain gene usage over developmental stages in the horse. Dev Comp Immunol. 2014;46:171–9.CrossRefPubMedPubMedCentral
9.
go back to reference Adderson EE, Shackelford PG, Quinn A, Carroll WL. Restricted Ig H chain V gene usage in the human antibody response to Haemophilus influenzae type b capsular polysaccharide. J Immunol. 1991;147:1667–74.PubMed Adderson EE, Shackelford PG, Quinn A, Carroll WL. Restricted Ig H chain V gene usage in the human antibody response to Haemophilus influenzae type b capsular polysaccharide. J Immunol. 1991;147:1667–74.PubMed
10.
go back to reference Adderson EE, Shackelford PG, Insel RA, Quinn A, Wilson PM, Carroll WL. Immunoglobulin light chain variable region gene sequences for human antibodies to Haemophilus influenzae type b capsular polysaccharide are dominated by a limited number of V kappa and V lambda segments and VJ combinations. J Clin Invest. 1992;89:729–38.CrossRefPubMedPubMedCentral Adderson EE, Shackelford PG, Insel RA, Quinn A, Wilson PM, Carroll WL. Immunoglobulin light chain variable region gene sequences for human antibodies to Haemophilus influenzae type b capsular polysaccharide are dominated by a limited number of V kappa and V lambda segments and VJ combinations. J Clin Invest. 1992;89:729–38.CrossRefPubMedPubMedCentral
11.
go back to reference Adderson EE, Shackelford PG, Quinn A, Wilson PM, Carroll WL. Diversity of immunoglobulin light chain usage in the human immune response to Haemophilus influenzae type b capsular polysaccharide. Pediatr Res. 1993;33:307–11.CrossRefPubMed Adderson EE, Shackelford PG, Quinn A, Wilson PM, Carroll WL. Diversity of immunoglobulin light chain usage in the human immune response to Haemophilus influenzae type b capsular polysaccharide. Pediatr Res. 1993;33:307–11.CrossRefPubMed
12.
go back to reference Houimel M. The analysis of VH and VL genes repertoires of Fab library built from peripheral B cells of human rabies virus vaccinated donors. Hum Immunol. 2014;75:745–55.CrossRefPubMed Houimel M. The analysis of VH and VL genes repertoires of Fab library built from peripheral B cells of human rabies virus vaccinated donors. Hum Immunol. 2014;75:745–55.CrossRefPubMed
13.
go back to reference Cho MJ, Lo AS, Mao X, Nagler AR, Ellebrecht CT, Mukherjee EM, et al. Shared VH1-46 gene usage by pemphigus vulgaris autoantibodies indicates common humoral immune responses among patients. Nat Commun. 2014;5:4167.PubMedPubMedCentral Cho MJ, Lo AS, Mao X, Nagler AR, Ellebrecht CT, Mukherjee EM, et al. Shared VH1-46 gene usage by pemphigus vulgaris autoantibodies indicates common humoral immune responses among patients. Nat Commun. 2014;5:4167.PubMedPubMedCentral
14.
17.
go back to reference Robinson J, Halliwell JA, Hayhurst JD, Flicek P, Parham P, Marsh SG. The IPD and IMGT/HLA database: allele variant databases. Nucleic Acids Res. 2015;43:D423–31.CrossRefPubMed Robinson J, Halliwell JA, Hayhurst JD, Flicek P, Parham P, Marsh SG. The IPD and IMGT/HLA database: allele variant databases. Nucleic Acids Res. 2015;43:D423–31.CrossRefPubMed
18.
19.
go back to reference Mroczek ES, Ippolito GC, Rogosch T, Hoi KH, Hwangpo TA, Brand MG, et al. Differences in the composition of the human antibody repertoire by B cell subsets in the blood. Front Immunol. 2014;5:96.CrossRefPubMedPubMedCentral Mroczek ES, Ippolito GC, Rogosch T, Hoi KH, Hwangpo TA, Brand MG, et al. Differences in the composition of the human antibody repertoire by B cell subsets in the blood. Front Immunol. 2014;5:96.CrossRefPubMedPubMedCentral
21.
go back to reference Hardy RR, Carmack CE, Li YS, Hayakawa K. Distinctive developmental origins and specificities of murine CD5+ B cells. Immunol Rev. 1994;137:91–118.CrossRefPubMed Hardy RR, Carmack CE, Li YS, Hayakawa K. Distinctive developmental origins and specificities of murine CD5+ B cells. Immunol Rev. 1994;137:91–118.CrossRefPubMed
22.
go back to reference Berland R, Wortis HH. Origins and functions of B-1 cells with notes on the role of CD5. Annu Rev Immunol. 2002;20:253–300.CrossRefPubMed Berland R, Wortis HH. Origins and functions of B-1 cells with notes on the role of CD5. Annu Rev Immunol. 2002;20:253–300.CrossRefPubMed
23.
go back to reference Kroese FG, de Waard R, Bos NA. B-1 cells and their reactivity with the murine intestinal microflora. Semin Immunol. 1996;8:11–8.CrossRefPubMed Kroese FG, de Waard R, Bos NA. B-1 cells and their reactivity with the murine intestinal microflora. Semin Immunol. 1996;8:11–8.CrossRefPubMed
24.
go back to reference Griffin DO, Holodick NE, Rothstein TL. Human B1 cells in umbilical cord and adult peripheral blood express the novel phenotype CD20+ CD27+ CD43+ CD70. J Exp Med. 2011;208:67–80.CrossRefPubMedPubMedCentral Griffin DO, Holodick NE, Rothstein TL. Human B1 cells in umbilical cord and adult peripheral blood express the novel phenotype CD20+ CD27+ CD43+ CD70. J Exp Med. 2011;208:67–80.CrossRefPubMedPubMedCentral
25.
go back to reference Irei T, Ohdan H, Zhou W, Ishiyama K, Tanaka Y, Ide K, et al. The persistent elimination of B cells responding to blood group a carbohydrates by synthetic group a carbohydrates and B-1 cell differentiation blockade: novel concept in preventing antibody-mediated rejection in ABO-incompatible transplantation. Blood. 2007;110:4567–75.CrossRefPubMed Irei T, Ohdan H, Zhou W, Ishiyama K, Tanaka Y, Ide K, et al. The persistent elimination of B cells responding to blood group a carbohydrates by synthetic group a carbohydrates and B-1 cell differentiation blockade: novel concept in preventing antibody-mediated rejection in ABO-incompatible transplantation. Blood. 2007;110:4567–75.CrossRefPubMed
26.
go back to reference Yoshikawa S, Kawano Y, Minegishi Y, Karasuyama H. The skewed heavy-chain repertoire in peritoneal B-1 cells is predetermined by the selection via pre-B cell receptor during B cell ontogeny in the fetal liver. Int Immunol. 2009;21:43–52.CrossRefPubMed Yoshikawa S, Kawano Y, Minegishi Y, Karasuyama H. The skewed heavy-chain repertoire in peritoneal B-1 cells is predetermined by the selection via pre-B cell receptor during B cell ontogeny in the fetal liver. Int Immunol. 2009;21:43–52.CrossRefPubMed
27.
go back to reference Vincent B, Buntzman A, Hopson B, McEwen C, Cowell L, Akoglu A, et al. iWAS--A novel approach to analyzing next generation sequence data for immunology. Cell Immunol. 2016;299:6–13.CrossRefPubMed Vincent B, Buntzman A, Hopson B, McEwen C, Cowell L, Akoglu A, et al. iWAS--A novel approach to analyzing next generation sequence data for immunology. Cell Immunol. 2016;299:6–13.CrossRefPubMed
Metadata
Title
VDJ gene usage among B-cell receptors in ABO-incompatible kidney transplantation determined by RNA-seq Transcriptomic analysis
Authors
Hee Jung Jeon
Kwangsoo Kim
Jae-Ghi Lee
Joon Young Jang
Seongmin Choi
Taishi Fang
Ji-Jing Yan
Miyeun Han
Jong Cheol Jeong
Kyoung-Bun Lee
Tae Jin Kim
Curie Ahn
Jaeseok Yang
Publication date
01-12-2017
Publisher
BioMed Central
Published in
BMC Nephrology / Issue 1/2017
Electronic ISSN: 1471-2369
DOI
https://doi.org/10.1186/s12882-017-0770-8

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