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Treatment of aggressive T-cell lymphoma/leukemia with anti-CD4 CAR T cells.
Feng, Jia; Xu, Haichan; Cinquina, Andrew; Wu, Zehua; Zhang, Wenli; Sun, Lihua; Chen, Qi; Tian, Lei; Song, Le; Pinz, Kevin G; Wada, Masayuki; Jiang, Xun; Hanes, William M; Ma, Yupo; Zhang, Hongyu.
Afiliação
  • Feng J; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Xu H; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Cinquina A; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Wu Z; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Zhang W; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Sun L; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Chen Q; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
  • Tian L; Department of Hematology, Peking University Third Hospital, Beijing, China.
  • Song L; Department of Nuclear Medicine, Peking University Third Hospital, Beijing, China.
  • Pinz KG; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Wada M; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Jiang X; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Hanes WM; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Ma Y; iCell Gene Therapeutics LLC, Research & Development Division, Long Island High Technology Incubator, Stony Brook, NY, United States.
  • Zhang H; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Front Immunol ; 13: 997482, 2022.
Article em En | MEDLINE | ID: mdl-36172388
ABSTRACT
T-cell lymphomas are aggressive lymphomas that often resist current therapy options or present with relapsed disease, making the development of more effective treatment regimens clinically important. Previously, we have shown that CD4 CAR can effectively target T-cell malignancies in preclinical studies. As IL-15 has been shown to strengthen the anti-tumor response, we have modified CD4 CAR to secrete an IL-15/IL-15sushi complex. These CD4-IL15/IL15sushi CAR T cells and NK92 cells efficiently eliminated CD4+ leukemic cell lines in co-culture assays. Additionally, CD4-IL15/IL15sushi CAR out-performed CD4 CAR in in vivo models, demonstrating a benefit to IL-15/IL-15sushi inclusion. In a Phase I clinical trial, CD4-IL15/IL15sushi CAR T cells were tested for safety in three patients with different T-cell lymphomas. Infusion of CD4-IL15/IL15sushi CAR T cells was well-tolerated by the patients without significant adverse effects and led to the remission of their lymphomas. Additionally, infusion led to the depletion of CD4+ Treg cells and expansion of CD3+CD8+ T cells and NK cells. These results suggest that CD4-IL15/IL15sushi CAR T cells may be a safe and effective treatment for patients with relapsed or refractory T-cell lymphomas, where new treatment options are needed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia / Linfoma de Células T Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia / Linfoma de Células T Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article