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        <datestamp>2026-09-14T05:43:01Z</datestamp>
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          <dc:title>Data Sheet 1_Dynamic γδ T-cell Receptor remodeling and antigen-induced T-cell IFN-γ responses after SARS-CoV-2 infection during pregnancy: insights for γδ T-cell immunotherapy.docx</dc:title>
          <dc:creator>Yuhan Ke (14822515)</dc:creator>
          <dc:creator>Rongfeng Pan (24868465)</dc:creator>
          <dc:creator>Ling Li (38566)</dc:creator>
          <dc:creator>Jing He (58446)</dc:creator>
          <dc:creator>Yafang Li (125524)</dc:creator>
          <dc:creator>Yuyuan Chen (7460660)</dc:creator>
          <dc:creator>Hongjie Liu (285479)</dc:creator>
          <dc:creator>Jiawei Li (559407)</dc:creator>
          <dc:creator>Muzi Luo (24868468)</dc:creator>
          <dc:creator>Rong Guo (50063)</dc:creator>
          <dc:creator>Yan Chen (4308)</dc:creator>
          <dc:creator>Danchun Chen (24868474)</dc:creator>
          <dc:creator>Chengfang Xu (18323413)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>IFN-γ</dc:subject>
          <dc:subject>maternal-fetal immunity</dc:subject>
          <dc:subject>PD-1</dc:subject>
          <dc:subject>pregnancy</dc:subject>
          <dc:subject>receptor remodeling</dc:subject>
          <dc:subject>SARS-CoV-2</dc:subject>
          <dc:subject>T-cell immunotherapy</dc:subject>
          <dc:subject>γδ-T cells</dc:subject>
          <dc:description>Introduction&lt;p&gt;Pregnancy requires coordinated immune adaptation to maintain fetal tolerance while preserving antiviral defense. However, the temporal dynamics of maternal cellular immunity and maternal-fetal antibody transfer after SARS-CoV-2 infection during pregnancy remain incompletely defined.&lt;/p&gt;Methods&lt;p&gt;We enrolled 52 pregnant women with laboratory-confirmed SARS-CoV-2 infection and stratified them by infection-to-delivery interval: &lt;90 days, 90–120 days, and &gt;120 days. Maternal peripheral blood mononuclear cells were analyzed by multiparametric flow cytometry. Basal and Omicron BA.5.2 antigen-induced IFN-γ production by CD3&lt;sup&gt;+&lt;/sup&gt;, CD4&lt;sup&gt;+&lt;/sup&gt;, and CD8&lt;sup&gt;+&lt;/sup&gt; T cells were assessed, and SARS-CoV-2-specific S1/RBD IgM and IgG levels were measured in paired maternal and cord blood by ELISA.&lt;/p&gt;Results&lt;p&gt;Baseline characteristics and major perinatal outcomes were broadly comparable among groups. Maternal T cells retained antigen-inducible IFN-γ responses, with the strongest responses observed in the 90–120-day group. Immune phenotyping revealed interval-associated remodeling of adaptive T-cell subsets, γδ T-cell receptor phenotypes, NK-cell subsets, and selected B-cell compartments. Cord blood IgM remained consistently low, providing no immunological evidence of intrauterine SARS-CoV-2 infection. In contrast, maternal and cord blood IgG levels were positively correlated, indicating preserved transplacental IgG transfer without clear time-dependent changes in transfer efficiency.&lt;/p&gt;Conclusions&lt;p&gt;These results extend current understanding of post-infection immune adaptation during pregnancy and provide an immunological basis for future longitudinal studies aimed at defining the timing and durability of maternal and neonatal immune protection.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T05:43:01Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1914308</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Dynamic_T-cell_Receptor_remodeling_and_antigen-induced_T-cell_IFN-_responses_after_SARS-CoV-2_infection_during_pregnancy_insights_for_T-cell_immunotherapy_docx/33719200</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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