<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Eissa H</submitter><funding>Intramural NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>287-296</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11294800</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>153(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The Primary Immune Deficiency Treatment Consortium (PIDTC) enrolled children in the United States and Canada onto a retrospective multicenter natural history study of hematopoietic cell transplantation (HCT).&lt;h4>Objective&lt;/h4>We investigated outcomes of HCT for severe combined immunodeficiency (SCID).&lt;h4>Methods&lt;/h4>We evaluated the chronic and late effects (CLE) after HCT for SCID in 399 patients transplanted from 1982 to 2012 at 32 PIDTC centers. Eligibility criteria included survival to at least 2 years after HCT without need for subsequent cellular therapy. CLE were defined as either conditions present at any time before 2 years from HCT that remained unresolved (chronic), or new conditions that developed beyond 2 years after HCT (late).&lt;h4>Results&lt;/h4>The cumulative</pubmed_abstract><journal>The Journal of allergy and clinical immunology</journal><pubmed_title>Posttransplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study.</pubmed_title><pmcid>PMC11294800</pmcid><funding_grant_id>U01 AI126612</funding_grant_id><funding_grant_id>ZIA AI001222</funding_grant_id><funding_grant_id>P30 CA042014</funding_grant_id><funding_grant_id>U10 HL069254</funding_grant_id><funding_grant_id>UL1 TR002494</funding_grant_id><funding_grant_id>UG1 HL069254</funding_grant_id><funding_grant_id>KL2 TR002492</funding_grant_id><funding_grant_id>U01 TR001263</funding_grant_id><funding_grant_id>U54 AI082973</funding_grant_id><funding_grant_id>U54 NS064808</funding_grant_id><pubmed_authors>Griffith LM</pubmed_authors><pubmed_authors>Pai SY</pubmed_authors><pubmed_authors>Burroughs LM</pubmed_authors><pubmed_authors>Bednarski JJ</pubmed_authors><pubmed_authors>Haddad E</pubmed_authors><pubmed_authors>Logan BR</pubmed_authors><pubmed_authors>Buckley RH</pubmed_authors><pubmed_authors>Chaudhury S</pubmed_authors><pubmed_authors>Abdel-Azim H</pubmed_authors><pubmed_authors>Prockop S</pubmed_authors><pubmed_authors>Goldman F</pubmed_authors><pubmed_authors>Dong H</pubmed_authors><pubmed_authors>O'Reilly RJ</pubmed_authors><pubmed_authors>Shereck E</pubmed_authors><pubmed_authors>Malech HL</pubmed_authors><pubmed_authors>Gillio AP</pubmed_authors><pubmed_authors>Quinones R</pubmed_authors><pubmed_authors>Oved JH</pubmed_authors><pubmed_authors>Kohn DB</pubmed_authors><pubmed_authors>Dara J</pubmed_authors><pubmed_authors>Molinari L</pubmed_authors><pubmed_authors>Heimall J</pubmed_authors><pubmed_authors>Knutsen A</pubmed_authors><pubmed_authors>Jyonouchi SC</pubmed_authors><pubmed_authors>DeSantes K</pubmed_authors><pubmed_authors>Mousallem TI</pubmed_authors><pubmed_authors>Notarangelo LD</pubmed_authors><pubmed_authors>Ebens CL</pubmed_authors><pubmed_authors>Leiding J</pubmed_authors><pubmed_authors>Cowan MJ</pubmed_authors><pubmed_authors>Parrott RE</pubmed_authors><pubmed_authors>Bleesing JH</pubmed_authors><pubmed_authors>Thakar MS</pubmed_authors><pubmed_authors>Martinez C</pubmed_authors><pubmed_authors>Dorsey M</pubmed_authors><pubmed_authors>Yu LC</pubmed_authors><pubmed_authors>Pulsipher MA</pubmed_authors><pubmed_authors>Rozmus J</pubmed_authors><pubmed_authors>Moore TB</pubmed_authors><pubmed_authors>Rayes A</pubmed_authors><pubmed_authors>Broglie L</pubmed_authors><pubmed_authors>Puck JM</pubmed_authors><pubmed_authors>Forbes Satter L</pubmed_authors><pubmed_authors>Shah AJ</pubmed_authors><pubmed_authors>Chandra S</pubmed_authors><pubmed_authors>Marsh RA</pubmed_authors><pubmed_authors>Eissa H</pubmed_authors><pubmed_authors>Kapoor N</pubmed_authors><pubmed_authors>Chandrakasan S</pubmed_authors><pubmed_authors>Cuvelier GDE</pubmed_authors><pubmed_authors>Davila Saldana BJ</pubmed_authors><pubmed_authors>Chellapandian D</pubmed_authors><pubmed_authors>Kapadia M</pubmed_authors><pubmed_authors>Torgerson T</pubmed_authors><pubmed_authors>Vander Lugt MT</pubmed_authors><pubmed_authors>Aquino V</pubmed_authors><pubmed_authors>Teira P</pubmed_authors><pubmed_authors>Dvorak CC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Posttransplantation late complications increase over time for patients with SCID: A Primary Immune Deficiency Treatment Consortium (PIDTC) landmark study.</name><description>&lt;h4>Background&lt;/h4>The Primary Immune Deficiency Treatment Consortium (PIDTC) enrolled children in the United States and Canada onto a retrospective multicenter natural history study of hematopoietic cell transplantation (HCT).&lt;h4>Objective&lt;/h4>We investigated outcomes of HCT for severe combined immunodeficiency (SCID).&lt;h4>Methods&lt;/h4>We evaluated the chronic and late effects (CLE) after HCT for SCID in 399 patients transplanted from 1982 to 2012 at 32 PIDTC centers. Eligibility criteria included survival to at least 2 years after HCT without need for subsequent cellular therapy. CLE were defined as either conditions present at any time before 2 years from HCT that remained unresolved (chronic), or new conditions that developed beyond 2 years after HCT (late).&lt;h4>Results&lt;/h4>The cumulative</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2026-06-02T13:09:11.546Z</modification><creation>2026-04-18T03:11:21.34Z</creation></dates><accession>S-EPMC11294800</accession><cross_references><pubmed>37793572</pubmed><doi>10.1016/j.jaci.2023.09.027</doi></cross_references></HashMap>