<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>An L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>For CD19-positive relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL) after treatment with murine CD19 (mCD19) CAR-T, the reinfusion of mCD19 CAR-T cells may be ineffective due to anti-mouse single-chain variable fragment (scFv) antibody caused by mCD19 CAR. To overcome this immunogenicity, we applied humanized CD19 (hCD19) CAR-T cells to treat r/r B-ALL patients with prior mCD19 CAR-T therapy.&lt;h4>Methods&lt;/h4>Nineteen pediatric and adult patients were included, 16 relapsed after and 3 were primarily resistant to mCD19 CAR-T. All patients presented with more than 5% blasts in bone marrow and/or extramedullary disease, and still showed CD19 antigen expression. Humanized CD19-CARs were lentiviral vectors carrying a second generation CAR with 4-1-BB co-stimul</pubmed_abstract><journal>BMC cancer</journal><pagination>393</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9004014</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Humanized CD19 CAR-T cells in relapsed/refractory B-ALL patients who relapsed after or failed murine CD19 CAR-T therapy.</pubmed_title><pmcid>PMC9004014</pmcid><pubmed_authors>Deng B</pubmed_authors><pubmed_authors>Tong C</pubmed_authors><pubmed_authors>An L</pubmed_authors><pubmed_authors>Chang AH</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Zhao D</pubmed_authors><pubmed_authors>Ling Z</pubmed_authors><pubmed_authors>Wu T</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Humanized CD19 CAR-T cells in relapsed/refractory B-ALL patients who relapsed after or failed murine CD19 CAR-T therapy.</name><description>&lt;h4>Background&lt;/h4>For CD19-positive relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL) after treatment with murine CD19 (mCD19) CAR-T, the reinfusion of mCD19 CAR-T cells may be ineffective due to anti-mouse single-chain variable fragment (scFv) antibody caused by mCD19 CAR. To overcome this immunogenicity, we applied humanized CD19 (hCD19) CAR-T cells to treat r/r B-ALL patients with prior mCD19 CAR-T therapy.&lt;h4>Methods&lt;/h4>Nineteen pediatric and adult patients were included, 16 relapsed after and 3 were primarily resistant to mCD19 CAR-T. All patients presented with more than 5% blasts in bone marrow and/or extramedullary disease, and still showed CD19 antigen expression. Humanized CD19-CARs were lentiviral vectors carrying a second generation CAR with 4-1-BB co-stimul</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-21T17:33:17.397Z</modification><creation>2025-04-05T16:40:40.543Z</creation></dates><accession>S-EPMC9004014</accession><cross_references><pubmed>35410148</pubmed><doi>10.1186/s12885-022-09489-1</doi></cross_references></HashMap>