<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zeng S</submitter><funding>NIAID NIH HHS</funding><funding>NIAID</funding><pagination>1511-1525</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11228286</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(10)</volume><pubmed_abstract>Human leukocyte antigen antibodies are important immunologic mediators of renal allograft loss and are difficult to control. The inability to permanently eliminate donor-specific antibodies (DSA) is partly due to an incomplete understanding of the cellular mechanisms driving alloantibody formation, recurrence, and maintenance. Memory T follicular helper (mTfh) cells rapidly interact with memory B cells upon antigen re-exposure for anamnestic humoral responses, but little is known about Tfh memory in transplantation. We hypothesized that alloreactive mTfh cells form after transplantation and play a critical role in DSA formation following alloantigen re-encounter. To test this hypothesis, we utilized murine skin allograft models to identify and characterize Tfh memory and interrogate its ab</pubmed_abstract><journal>American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons</journal><pubmed_title>Memory T follicular helper cells drive donor-specific antibodies independent of memory B cells and primary germinal center and alloantibody formation.</pubmed_title><pmcid>PMC11228286</pmcid><funding_grant_id>R01 AI164716</funding_grant_id><funding_grant_id>T32 AI070081</funding_grant_id><funding_grant_id>K08 AI132747</funding_grant_id><pubmed_authors>Zeng S</pubmed_authors><pubmed_authors>Ford ML</pubmed_authors><pubmed_authors>Crichton ES</pubmed_authors><pubmed_authors>Badell IR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Memory T follicular helper cells drive donor-specific antibodies independent of memory B cells and primary germinal center and alloantibody formation.</name><description>Human leukocyte antigen antibodies are important immunologic mediators of renal allograft loss and are difficult to control. The inability to permanently eliminate donor-specific antibodies (DSA) is partly due to an incomplete understanding of the cellular mechanisms driving alloantibody formation, recurrence, and maintenance. Memory T follicular helper (mTfh) cells rapidly interact with memory B cells upon antigen re-exposure for anamnestic humoral responses, but little is known about Tfh memory in transplantation. We hypothesized that alloreactive mTfh cells form after transplantation and play a critical role in DSA formation following alloantigen re-encounter. To test this hypothesis, we utilized murine skin allograft models to identify and characterize Tfh memory and interrogate its ab</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2025-04-18T12:58:15.372Z</modification><creation>2025-04-06T22:24:34.945Z</creation></dates><accession>S-EPMC11228286</accession><cross_references><pubmed>37302575</pubmed><doi>10.1016/j.ajt.2023.06.006</doi></cross_references></HashMap>