Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Mar-Apr;42(2):175-188.
doi: 10.1016/j.currproblcancer.2018.04.001. Epub 2018 Apr 22.

Gearing up T-cell immunotherapy in cervical cancer

Affiliations
Review

Gearing up T-cell immunotherapy in cervical cancer

Shilpa Raghuvanshi Chauhan et al. Curr Probl Cancer. 2018 Mar-Apr.

Abstract

The World Health Organization estimates more than 270,000 deaths annually by cervical cancer. Present vaccines are prophylactic in nature which cannot treat huge bulk of cervical cancer patients worldwide. Available therapies like radiotherapy, chemotherapy, or surgery are not effective in high-grade lesion, and hence, there is an unmet medical need for an effective form of therapy. T cells play a significant role in cervical cancer pathogenesis as human papilloma virus uses multiple mechanisms that dodge host T-cell immune-surveillance aiding in persistence of infection and establishment of cancer. Therefore, T-cell-based immunotherapy is gaining momentum since it is more specific and is entitled with broader therapeutic potential. This review outlines various ongoing research and trials in field of T-cell immunotherapy for treating cervical cancer using different fundamental strategies. It is becoming an important pharmacological tool and therapeutic option against cervical disease, as more and more studies are extending from preclinical studies to human trials.

Keywords: Cervical cancer; Human papilloma virus; Immunotherapy; T cells.

PubMed Disclaimer

MeSH terms

Substances