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B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy

BACKGROUND: Kidney transplantation is the most effective treatment for end-stage renal disease. Sensitization refers to pre-existing antibodies against human leukocyte antigen (HLA) protein and remains a major barrier to successful transplantation. Despite implementation of desensitization strategie...

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Autores principales: Beausang, John F., Fan, H. Christina, Sit, Rene, Hutchins, Maria U., Jirage, Kshama, Curtis, Rachael, Hutchins, Edward, Quake, Stephen R., Yabu, Julie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237299/
https://www.ncbi.nlm.nih.gov/pubmed/28086979
http://dx.doi.org/10.1186/s12967-017-1118-7
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author Beausang, John F.
Fan, H. Christina
Sit, Rene
Hutchins, Maria U.
Jirage, Kshama
Curtis, Rachael
Hutchins, Edward
Quake, Stephen R.
Yabu, Julie M.
author_facet Beausang, John F.
Fan, H. Christina
Sit, Rene
Hutchins, Maria U.
Jirage, Kshama
Curtis, Rachael
Hutchins, Edward
Quake, Stephen R.
Yabu, Julie M.
author_sort Beausang, John F.
collection PubMed
description BACKGROUND: Kidney transplantation is the most effective treatment for end-stage renal disease. Sensitization refers to pre-existing antibodies against human leukocyte antigen (HLA) protein and remains a major barrier to successful transplantation. Despite implementation of desensitization strategies, many candidates fail to respond. Our objective was to determine whether measuring B cell repertoires could differentiate candidates that respond to desensitization therapy. METHODS: We developed an assay based on high-throughput DNA sequencing of the variable domain of the heavy chain of immunoglobulin genes to measure changes in B cell repertoires in 19 highly HLA-sensitized kidney transplant candidates undergoing desensitization and 7 controls with low to moderate HLA sensitization levels. Responders to desensitization had a decrease of 5% points or greater in cumulated calculated panel reactive antibody (cPRA) levels, and non-responders had no decrease in cPRA. RESULTS: Dominant B cell clones were not observed in highly sensitized candidates, suggesting that the B cells responsible for sensitization are either not present in peripheral blood or present at comparable levels to other circulating B cells. Candidates that responded to desensitization therapy had pre-treatment repertoires composed of a larger fraction of class-switched (IgG and IgA) isotypes compared to non-responding candidates. After B cell depleting therapy, the proportion of switched isotypes increased and the mutation frequencies of the remaining non-switched isotypes (IgM and IgD) increased in both responders and non-responders, perhaps representing a shift in the repertoire towards memory B cells or plasmablasts. Conversely, after transplantation, non-switched isotypes with fewer mutations increased, suggesting a shift in the repertoire towards naïve B cells. CONCLUSIONS: Relative abundance of different B cell isotypes is strongly perturbed by desensitization therapy and transplantation, potentially reflecting changes in the relative abundance of memory and naïve B cell compartments. Candidates that responded to therapy experienced similar changes to those that did not respond. Further studies are required to understand differences between these two groups of highly sensitized kidney transplant candidates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-017-1118-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-52372992017-01-18 B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy Beausang, John F. Fan, H. Christina Sit, Rene Hutchins, Maria U. Jirage, Kshama Curtis, Rachael Hutchins, Edward Quake, Stephen R. Yabu, Julie M. J Transl Med Research BACKGROUND: Kidney transplantation is the most effective treatment for end-stage renal disease. Sensitization refers to pre-existing antibodies against human leukocyte antigen (HLA) protein and remains a major barrier to successful transplantation. Despite implementation of desensitization strategies, many candidates fail to respond. Our objective was to determine whether measuring B cell repertoires could differentiate candidates that respond to desensitization therapy. METHODS: We developed an assay based on high-throughput DNA sequencing of the variable domain of the heavy chain of immunoglobulin genes to measure changes in B cell repertoires in 19 highly HLA-sensitized kidney transplant candidates undergoing desensitization and 7 controls with low to moderate HLA sensitization levels. Responders to desensitization had a decrease of 5% points or greater in cumulated calculated panel reactive antibody (cPRA) levels, and non-responders had no decrease in cPRA. RESULTS: Dominant B cell clones were not observed in highly sensitized candidates, suggesting that the B cells responsible for sensitization are either not present in peripheral blood or present at comparable levels to other circulating B cells. Candidates that responded to desensitization therapy had pre-treatment repertoires composed of a larger fraction of class-switched (IgG and IgA) isotypes compared to non-responding candidates. After B cell depleting therapy, the proportion of switched isotypes increased and the mutation frequencies of the remaining non-switched isotypes (IgM and IgD) increased in both responders and non-responders, perhaps representing a shift in the repertoire towards memory B cells or plasmablasts. Conversely, after transplantation, non-switched isotypes with fewer mutations increased, suggesting a shift in the repertoire towards naïve B cells. CONCLUSIONS: Relative abundance of different B cell isotypes is strongly perturbed by desensitization therapy and transplantation, potentially reflecting changes in the relative abundance of memory and naïve B cell compartments. Candidates that responded to therapy experienced similar changes to those that did not respond. Further studies are required to understand differences between these two groups of highly sensitized kidney transplant candidates. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-017-1118-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-13 /pmc/articles/PMC5237299/ /pubmed/28086979 http://dx.doi.org/10.1186/s12967-017-1118-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Beausang, John F.
Fan, H. Christina
Sit, Rene
Hutchins, Maria U.
Jirage, Kshama
Curtis, Rachael
Hutchins, Edward
Quake, Stephen R.
Yabu, Julie M.
B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title_full B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title_fullStr B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title_full_unstemmed B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title_short B cell repertoires in HLA-sensitized kidney transplant candidates undergoing desensitization therapy
title_sort b cell repertoires in hla-sensitized kidney transplant candidates undergoing desensitization therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237299/
https://www.ncbi.nlm.nih.gov/pubmed/28086979
http://dx.doi.org/10.1186/s12967-017-1118-7
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