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Black African and Latino/a identity correlates with increased plasmablasts in MS

OBJECTIVE: To determine the influence of self-reported Black African and Latin American identity on peripheral blood antibody-secreting cell (ASC) frequency in the context of relapsing-remitting MS. METHODS: In this cross-sectional study, we recruited 74 subjects with relapsing-remitting MS and 24 a...

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Autores principales: Telesford, Kiel M., Kaunzner, Ulrike W., Perumal, Jai, Gauthier, Susan A., Wu, Xian, Diaz, Ivan, Kruse-Hoyer, Mason, Engel, Casey, Marcille, Melanie, Vartanian, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865850/
https://www.ncbi.nlm.nih.gov/pubmed/31672834
http://dx.doi.org/10.1212/NXI.0000000000000634
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author Telesford, Kiel M.
Kaunzner, Ulrike W.
Perumal, Jai
Gauthier, Susan A.
Wu, Xian
Diaz, Ivan
Kruse-Hoyer, Mason
Engel, Casey
Marcille, Melanie
Vartanian, Timothy
author_facet Telesford, Kiel M.
Kaunzner, Ulrike W.
Perumal, Jai
Gauthier, Susan A.
Wu, Xian
Diaz, Ivan
Kruse-Hoyer, Mason
Engel, Casey
Marcille, Melanie
Vartanian, Timothy
author_sort Telesford, Kiel M.
collection PubMed
description OBJECTIVE: To determine the influence of self-reported Black African and Latin American identity on peripheral blood antibody-secreting cell (ASC) frequency in the context of relapsing-remitting MS. METHODS: In this cross-sectional study, we recruited 74 subjects with relapsing-remitting MS and 24 age-, and self-reported ethno-ancestral identity-matched healthy donors (HDs) to provide peripheral blood study samples. Subjects with MS were either off therapy at the time of study draw or on monthly natalizumab therapy infusions. Using flow cytometry, we assessed peripheral blood mononuclear cells for antibody-secreting B-cell subsets. RESULTS: When stratified by self-reported ethno-ancestry, we identified significantly elevated frequencies of circulating plasmablasts among individuals with MS identifying as Black African or Latin American relative to those of Caucasian ancestry. Ethno-ancestry–specific differences in ASC frequency were observed only among individuals with MS. By contrast, this differential was not observed among HDs. ASCs linked with poorer MS prognosis and active disease, including IgM(+)- and class-switched CD138(+) subsets, were among those significantly increased. CONCLUSION: The enhanced peripheral blood plasmablast signature revealed among Black African or Latin American subjects with MS points to distinct underlying mechanisms associated with MS immunopathogenesis. This dysregulation may contribute to the disease disparity experienced by patient populations of Black African or Latin American ethno-ancestry.
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spelling pubmed-68658502019-12-13 Black African and Latino/a identity correlates with increased plasmablasts in MS Telesford, Kiel M. Kaunzner, Ulrike W. Perumal, Jai Gauthier, Susan A. Wu, Xian Diaz, Ivan Kruse-Hoyer, Mason Engel, Casey Marcille, Melanie Vartanian, Timothy Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To determine the influence of self-reported Black African and Latin American identity on peripheral blood antibody-secreting cell (ASC) frequency in the context of relapsing-remitting MS. METHODS: In this cross-sectional study, we recruited 74 subjects with relapsing-remitting MS and 24 age-, and self-reported ethno-ancestral identity-matched healthy donors (HDs) to provide peripheral blood study samples. Subjects with MS were either off therapy at the time of study draw or on monthly natalizumab therapy infusions. Using flow cytometry, we assessed peripheral blood mononuclear cells for antibody-secreting B-cell subsets. RESULTS: When stratified by self-reported ethno-ancestry, we identified significantly elevated frequencies of circulating plasmablasts among individuals with MS identifying as Black African or Latin American relative to those of Caucasian ancestry. Ethno-ancestry–specific differences in ASC frequency were observed only among individuals with MS. By contrast, this differential was not observed among HDs. ASCs linked with poorer MS prognosis and active disease, including IgM(+)- and class-switched CD138(+) subsets, were among those significantly increased. CONCLUSION: The enhanced peripheral blood plasmablast signature revealed among Black African or Latin American subjects with MS points to distinct underlying mechanisms associated with MS immunopathogenesis. This dysregulation may contribute to the disease disparity experienced by patient populations of Black African or Latin American ethno-ancestry. Lippincott Williams & Wilkins 2019-10-31 /pmc/articles/PMC6865850/ /pubmed/31672834 http://dx.doi.org/10.1212/NXI.0000000000000634 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Telesford, Kiel M.
Kaunzner, Ulrike W.
Perumal, Jai
Gauthier, Susan A.
Wu, Xian
Diaz, Ivan
Kruse-Hoyer, Mason
Engel, Casey
Marcille, Melanie
Vartanian, Timothy
Black African and Latino/a identity correlates with increased plasmablasts in MS
title Black African and Latino/a identity correlates with increased plasmablasts in MS
title_full Black African and Latino/a identity correlates with increased plasmablasts in MS
title_fullStr Black African and Latino/a identity correlates with increased plasmablasts in MS
title_full_unstemmed Black African and Latino/a identity correlates with increased plasmablasts in MS
title_short Black African and Latino/a identity correlates with increased plasmablasts in MS
title_sort black african and latino/a identity correlates with increased plasmablasts in ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865850/
https://www.ncbi.nlm.nih.gov/pubmed/31672834
http://dx.doi.org/10.1212/NXI.0000000000000634
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