<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Matubu A</submitter><funding>NIAID NIH HHS</funding><pagination>e13210</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7900783</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>83(3)</volume><pubmed_abstract>&lt;h4>Problem&lt;/h4>Injectable contraceptive use may impact immune cell responsiveness and susceptibility to infection. We measured responsiveness of T-cells from women before and after initiating depot medroxyprogesterone acetate (DMPA) or norethisterone enanthate (Net-En).&lt;h4>Method of study&lt;/h4>Peripheral blood mononuclear cells collected from women aged 18-34 years prior to, at steady state, and nadir concentrations after initiating DMPA (n = 30) or Net-En (n = 36) and from women initiating copper intrauterine device (CU-IUD; n = 32) were stimulated with phorbol myristate acetate and analyzed using flow cytometry. We evaluated percentage change in T-cells expressing programmed cell death-1 (PD-1) and cytotoxic T-lymphocyte associated protein-4 (CTLA-4).&lt;h4>Results&lt;/h4>Compared to baseline, there were decreased numbers of CD4+CTLA4+ (P &lt; .001) and CD8+CTLA4+ (P &lt; .01) T-cells following ex vivo stimulation challenge at steady state DMPA concentrations and no differences at nadir concentrations (P = .781 and P = .463, respectively). In Net-En users, no differences in CD4+CTLA4+ T-cells at steady state (P = .087) and nadir concentrations (P = .217) were observed. DMPA users had fewer CD4+PD-1+ (P &lt; .001) and CD8+PD-1+ (P &lt; .001) T-cells at nadir concentrations. Number of CD4+PD-1+ and CD8+PD-1+ T-cells decreased at steady state concentration (P = .002 and P = .001, respectively) and at nadir concentrations after Net-En initiation (P &lt; .001 and P &lt; .001). In CU-IUD users, there were no changes in number of CD4+CTLA4+ (P = .426) and CD8+CTLA4+ (P = .169) and no changes in CD4+PD-1+ (P = .083) and CD8+PD-1+ (P = .936) compared to baseline.&lt;h4>Conclusion&lt;/h4>Activation of T-cells in response to ex vivo stimulation is suppressed at steady state DMPA concentration and resolves at nadir concentration, suggesting DMPA immunosuppressive effects may be transient.</pubmed_abstract><journal>American journal of reproductive immunology (New York, N.Y. : 1989)</journal><pubmed_title>Depot medroxyprogesterone acetate and norethisterone enanthate differentially impact T-cell responses and expression of immunosuppressive markers.</pubmed_title><pmcid>PMC7900783</pmcid><funding_grant_id>R01 AI102835</funding_grant_id><pubmed_authors>Matubu A</pubmed_authors><pubmed_authors>Mbizvo M</pubmed_authors><pubmed_authors>Chirenje ZM</pubmed_authors><pubmed_authors>Achilles SL</pubmed_authors><pubmed_authors>Mhlanga F</pubmed_authors><pubmed_authors>Maramba A</pubmed_authors><pubmed_authors>Meyn LA</pubmed_authors><pubmed_authors>Hillier SL</pubmed_authors><pubmed_authors>Stoner KA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Depot medroxyprogesterone acetate and norethisterone enanthate differentially impact T-cell responses and expression of immunosuppressive markers.</name><description>&lt;h4>Problem&lt;/h4>Injectable contraceptive use may impact immune cell responsiveness and susceptibility to infection. We measured responsiveness of T-cells from women before and after initiating depot medroxyprogesterone acetate (DMPA) or norethisterone enanthate (Net-En).&lt;h4>Method of study&lt;/h4>Peripheral blood mononuclear cells collected from women aged 18-34 years prior to, at steady state, and nadir concentrations after initiating DMPA (n = 30) or Net-En (n = 36) and from women initiating copper intrauterine device (CU-IUD; n = 32) were stimulated with phorbol myristate acetate and analyzed using flow cytometry. We evaluated percentage change in T-cells expressing programmed cell death-1 (PD-1) and cytotoxic T-lymphocyte associated protein-4 (CTLA-4).&lt;h4>Results&lt;/h4>Compared to baseline, there were decreased numbers of CD4+CTLA4+ (P &lt; .001) and CD8+CTLA4+ (P &lt; .01) T-cells following ex vivo stimulation challenge at steady state DMPA concentrations and no differences at nadir concentrations (P = .781 and P = .463, respectively). In Net-En users, no differences in CD4+CTLA4+ T-cells at steady state (P = .087) and nadir concentrations (P = .217) were observed. DMPA users had fewer CD4+PD-1+ (P &lt; .001) and CD8+PD-1+ (P &lt; .001) T-cells at nadir concentrations. Number of CD4+PD-1+ and CD8+PD-1+ T-cells decreased at steady state concentration (P = .002 and P = .001, respectively) and at nadir concentrations after Net-En initiation (P &lt; .001 and P &lt; .001). In CU-IUD users, there were no changes in number of CD4+CTLA4+ (P = .426) and CD8+CTLA4+ (P = .169) and no changes in CD4+PD-1+ (P = .083) and CD8+PD-1+ (P = .936) compared to baseline.&lt;h4>Conclusion&lt;/h4>Activation of T-cells in response to ex vivo stimulation is suppressed at steady state DMPA concentration and resolves at nadir concentration, suggesting DMPA immunosuppressive effects may be transient.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Mar</publication><modification>2024-11-20T07:47:50.396Z</modification><creation>2021-03-05T09:06:45Z</creation></dates><accession>S-EPMC7900783</accession><cross_references><pubmed>31729087</pubmed><doi>10.1111/aji.13210</doi></cross_references></HashMap>