<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-17T00:20:32Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/27058" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/27058</identifier><datestamp>2025-12-18T12:57:36Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">He, Chenfei</subfield>
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      <subfield code="a">Wang, Shan</subfield>
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      <subfield code="a">Moreews, Marion</subfield>
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      <subfield code="a">Pei, Shengduo</subfield>
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      <subfield code="a">Chen, Guangchun</subfield>
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      <subfield code="a">Li, Quan-Zhen</subfield>
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      <subfield code="a">Del Monte Monge, Alberto</subfield>
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      <subfield code="a">Ramiro, Almudena R</subfield>
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      <subfield code="a">Cai, Curtis</subfield>
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      <subfield code="a">Gaya, Mauro</subfield>
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      <subfield code="a">Barral, Patricia</subfield>
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      <subfield code="a">Buggert, Marcus</subfield>
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      <subfield code="a">Batista, Facundo D</subfield>
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      <subfield code="a">Karlsson, Mikael C I</subfield>
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      <subfield code="a">Invariant natural killer T (iNKT) cells are activated by glycolipids presented on CD1d. When iNKT cells interact with and activate B cells, they can differentiate into iNKT follicular helper (iNKTfh) cells, and here, we investigate how this, in turn, regulates conventional T follicular helper (Tfh) cells. This is done in an autoimmune model where antibodies are produced against self-antigens relevant to the autoimmune disease systemic lupus erythematosus (SLE). We find a balance between iNKTfh and Tfh cells that directs the B cell response and influences Tfh cell generation. This altered balance also affects the specificities and increases the autoantibody response. We also show that CD1d expression by B cells is essential for iNKTfh cell generation. In conclusion, our data shed light on how T cell help for B cells is divided between conventional and unconventional helper cell populations and how this has an impact on autoreactive B cell responses.</subfield>
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      <subfield code="a">Cell Rep. 2025 May 27;44(5):115602.</subfield>
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      <subfield code="a">CP: Immunology</subfield>
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      <subfield code="a">T follicular helper cells</subfield>
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      <subfield code="a">apoptotic cells</subfield>
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      <subfield code="a">The balance between conventional and unconventional T follicular helper cells influences autoreactive B cell responses.</subfield>
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