2022
DOI: 10.1016/j.humimm.2022.03.002
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A clinician’s guide to HLA matching in allogeneic hematopoietic stem cell transplant

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Cited by 13 publications
(8 citation statements)
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“…Also, evaluation for signs of immune tolerance breakdown, through the assessment of cellular subpopulations imbalance or its product (such as cytokines or chemokines) ( 128 ) and its correlation with known clinical signs of placental dysfunction (i.e., angiogenic markers or fetal & maternal Doppler), could also be explored. Moreover, HLA screening and matching could also be considered as a suitable tool attempting to decrease the reported immune tolerance disbalance ( 129 ).…”
Section: Discussionmentioning
confidence: 99%
“…Also, evaluation for signs of immune tolerance breakdown, through the assessment of cellular subpopulations imbalance or its product (such as cytokines or chemokines) ( 128 ) and its correlation with known clinical signs of placental dysfunction (i.e., angiogenic markers or fetal & maternal Doppler), could also be explored. Moreover, HLA screening and matching could also be considered as a suitable tool attempting to decrease the reported immune tolerance disbalance ( 129 ).…”
Section: Discussionmentioning
confidence: 99%
“…Donor–recipient HLA allele matching is an essential component of allogeneic hematopoietic stem cell transplant (HSCT) and high‐resolution HLA genotyping is routinely used for donor and recipient selection 1,2 . Here, we describe a novel HLA‐DRB1 allele, now officially named as HLA‐DRB1*11:283, that has been identified in a Chinese leukemia patient and his daughter.…”
Section: Figurementioning
confidence: 99%
“…The HLA genes are the most polymorphic in the human genome, which have evolved to allow the immune system to sense foreign pathogens and provide wide-ranging protection (18,19). The classical HLA genes are comprised of the Class I and Class II genes that present peptide antigen to T cells.…”
Section: Hla Antibodies In Hsctmentioning
confidence: 99%
“…Expression of Class II can be induced on other cell types, particularly in the setting of inflammation. Historically, HLA matching for HSCT patients and donors was performed for HLA-A, -B, -C, and -DR (8/8 loci matching), owing to limited typing methods that precluded typing at HLA-DQ and -DP (19). Currently, with the widespread and growing use of next-generation sequencing to perform genotyping, matching is clinically assessed at HLA-A, -B, -C, -DR, -DQ (10/10 loci matching) although data is available for donors and recipients at all HLA loci, including HLA-DP, -DRB345, -DQA1, and -DPA1.…”
Section: Hla Antibodies In Hsctmentioning
confidence: 99%