Neem leaf glycoprotein partially rectifies suppressed dendritic cell functions and associated T cell efficacy in stage IIIB cervical cancer patients
By: Roy S, Goswami S, Bose A, Chakraborty K, Pal S, Haldar A, Basu P, Biswas J, Baral R.

Departmant of Immunoregulation and Immunodiagnostics, Clinical Biochemistry Unit, Department of Gynaecological Oncology, Department of Surgical Oncology and Medical Oncology, Chittaranjan National Cancer Institute (CNCI), 37, S. P. Mukherjee Road, Kolkata 700026; India.
Clin Vaccine Immunol. 2011 Feb 9.

Abstract

Myeloid derived dendritic cells (DCs) generated from monocytes of Cervical Cancer, Stage IIIB (CaCx IIIB) patients show a dysfunctional maturation, and thus anti-tumor T cell functions are dysregulated. In an objective to optimize these dysregulated immune functions, the present study is focused on the ability of neem leaf glycoprotein (NLGP), a nontoxic preparation of neem leaf, to induce optimum maturation of dendritic cells from CaCx IIIB patients. In vitro NLGP treatment of immature DCs (iDCs) from CaCx IIIB patients results upregulated expression of various cell surface markers (CD40, CD83, CD80, CD86, HLA-ABC), which indicates DC maturation. Consequently, NLGP matured DCs displayed a balanced cytokine secretion with type 1 bias and noteworthy functional property. These DCs displayed substantial T cell allo-stimulatory capacity and promoted generation of cytotoxic T lymphocytes (CTLs). Although, NLGP matured DCs derived from CaCx monocytes is generally subdued compared to those from healthy monocyte origin, considerable revival of the suppressed DC based immune functions is noted in vitro at a fairly advanced stage of CaCx and, thus, further exploration of ex vivo and in vivo DC based vaccine is proposed. Moreover, DC maturating efficacy of NLGP might be much more effective in earlier stages of CaCx, where extent of immune dysregulation is less, thus, scope of further investigation may be explored.

PMID: 21307275 [PubMed - as supplied by publisher] Source: National Library of Medicine.







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