Junjun Chu

ORCID: 0000-0002-4916-5506
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About
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Research Areas
  • CAR-T cell therapy research
  • SARS-CoV-2 and COVID-19 Research
  • Long-Term Effects of COVID-19
  • Cancer Immunotherapy and Biomarkers
  • Immunotherapy and Immune Responses
  • COVID-19 Clinical Research Studies

University of Southern California
2024

Novartis (United States)
2022

T cell receptor (TCR)-engineered therapy is a promising potential treatment for solid tumors, with preliminary efficacy demonstrated in clinical trials. However, obtaining clinically effective TCR molecules remains major challenge. We have developed strategy cloning tumor-specific TCRs from long-term surviving patients who responded to immunotherapy. Here, we report the identification of (10F04), which human leukocyte antigen (HLA)-DRA/DRB1*09:01 restricted and papillomavirus type 18 (HPV18) E7

10.1038/s41467-024-46558-4 article EN cc-by Nature Communications 2024-03-13

Background: New therapies for multiple myeloma (MM) such as immunomodulatory drugs (IMiD), proteasome inhibitors (PI), and CD38-targeted monoclonal antibodies (anti-CD38 mAb) enhance the overall survival (OS) of patients (pts) with relapsed and/or refractory (r/r) MM. However, MM remains incurable, insufficient rates duration response, progression-free (PFS). B-cell maturation antigen (BCMA) is expressed in cells essential maintenance long-lived plasma cells. It a clinically validated target...

10.1097/01.hs9.0000850768.54900.41 article EN cc-by-nc-nd HemaSphere 2022-06-01
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