Relevance of antibodies in hematopoietic stem cell transplantation: Antibodies anti-HLA, anti-platelets, anti-granulocytes, anti-erythrocytes and anti-MICA. Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-

Affiliation auteurs!!!! Error affiliation !!!!
TitreRelevance of antibodies in hematopoietic stem cell transplantation: Antibodies anti-HLA, anti-platelets, anti-granulocytes, anti-erythrocytes and anti-MICA. Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-
Type de publicationJournal Article
Year of Publication2020
AuteursDelbos F, Blouin L, Bruno B, Crocchiolo R, Desoutter J, Detrait M, Nguyen-Lejarre KTien, Giannoli C, Lemarie C, Renac V, Yakoub-Agha I, Dubois V
JournalBULLETIN DU CANCER
Volume107
PaginationS159-S169
Date PublishedDEC
Type of ArticleArticle
ISSN0007-4551
Mots-clésantibodies, Hematopoietic stem cell, HLA, HNA, HPA, MICA, transplantation
Résumé

The presence of alto-antibodies in the serum of a recipient awaiting hematopoietic stem cell transplantation (HSCT) may hove an impact on transfusion efficiency and/or donor choice, especially in the absence of an identical sibling donor. Prior to transplantation, donor specific anti-HLA (Human Leukocyte Antigen) antibodies (OSA) have a recognized effect on transplant outcome, correlated with the increasing MR value and with the ability of such antibody to fix the complement fraction. Anti-platelet antibodies (anti-HLA class l and anti-HPA [Human Platelet Antigen]) are better involved in transfusion inefficiency and can be responsible for refractory status. ABO incompatibilities require a specific treatment of the graft in presence of high titer to avoid hemolytic adverse effects. Investigations of these antibodies should be carried out on a regular basis in order to establish appropriate transfusion recommendation, select an alternative donor when possible or adapt the source of cells. After transplantation, in case of delayed recovery or graft rejection, long term aplasia, persistent mixed chimerism or late release, and after elimination of the main clinical causes, a biological assessment targeted on the different type of antibodies will hove to be performed in order to orient towards the cause or the appropriate therapy. Further studies should be carried out to determine the impact of anti-MICA antibodies and recipient specific anti-HLA antibodies, on the outcome of the transplantation.

DOI10.1016/j.bulcan.2020.04.015