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Exploring cellular immunotherapy platforms in multiple myeloma.
Vo, Manh-Cuong; Jung, Sung-Hoon; Nguyen, Van-Tan; Tran, Van-Dinh-Huan; Ruzimurodov, Nodirjon; Kim, Sang Ki; Nguyen, Xuan-Hung; Kim, Mihee; Song, Ga-Young; Ahn, Seo-Yeon; Ahn, Jae-Sook; Yang, Deok-Hwan; Kim, Hyeoung-Joon; Lee, Je-Jung.
Afiliación
  • Vo MC; Institute of Research and Development, Duy Tan University, Danang, Viet Nam.
  • Jung SH; Research Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
  • Nguyen VT; Vaxcell-Bio Therapeutics, Hwasun, Jeollanamdo, Republic of Korea.
  • Tran VD; Research Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
  • Ruzimurodov N; Department of Hematology-Oncology, Chonnam National University Hwasun Hospital and Chonnam National University Medical School, Hwasun, Jeollanamdo, Republic of Korea.
  • Kim SK; Research Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
  • Nguyen XH; Research Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
  • Kim M; Institute of Immunology and Human Genomics of the Academy of Sciences of the Republic of Uzbekistan, Uzbekistan.
  • Song GY; Research Center for Cancer Immunotherapy, Chonnam National University Hwasun Hospital, Hwasun, Jeollanamdo, Republic of Korea.
  • Ahn SY; Department of Laboratory and Companion Animal Science, College of Industrial Science, Kongju National University, Yesan-eup, Yesan-gun, Chungnam, Republic of Korea.
  • Ahn JS; Vaxcell-Bio Therapeutics, Hwasun, Jeollanamdo, Republic of Korea.
  • Yang DH; Hi-Tech Center and Vinmec-VinUni Institute of Immunology, Vinmec Healthcare system, Hanoi, Vietnam.
  • Kim HJ; Department of Hematology-Oncology, Chonnam National University Hwasun Hospital and Chonnam National University Medical School, Hwasun, Jeollanamdo, Republic of Korea.
  • Lee JJ; Department of Hematology-Oncology, Chonnam National University Hwasun Hospital and Chonnam National University Medical School, Hwasun, Jeollanamdo, Republic of Korea.
Heliyon ; 10(6): e27892, 2024 Mar 30.
Article en En | MEDLINE | ID: mdl-38524535
ABSTRACT
Despite major advances in therapeutic platforms, most patients with multiple myeloma (MM) eventually relapse and succumb to the disease. Among the novel therapeutic options developed over the past decade, genetically engineered T cells have a great deal of potential. Cellular immunotherapies, including chimeric antigen receptor (CAR) T cells, are rapidly becoming an effective therapeutic modality for MM. Marrow-infiltrating lymphocytes (MILs) derived from the bone marrow of patients with MM are a novel source of T cells for adoptive T-cell therapy, which robustly and specifically target myeloma cells. In this review, we examine the recent innovations in cellular immunotherapies, including the use of dendritic cells, and cellular tools based on MILs, natural killer (NK) cells, and CAR T cells, which hold promise for improving the efficacy and/or reducing the toxicity of treatment in patients with MM.
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