Modified DCs and MSCs with HPV E7 antigen and small Hsps: Which one is the most potent strategy for eradication of tumors?. (April 2019)

• Record Type: Journal Article
• Authors: Bolhassani, Azam; Shahbazi, Sepideh; Agi, Elnaz; Haghighipour, Nooshin; Hadi, Amin; Asgari, Fatemeh
• Is Part Of: Molecular immunology. Volume 108(2019:Apr.)
• Page Start: 102
• Page End: 110
• Publication Date: 2019-04
• Subjects: APC antigen presenting cell -- DC dendritic cell -- MSC mesenchymal stem cell -- HPV human papillomavirus -- Hsp heat shock protein -- sHsp small heat shock protein -- HCV hepatitis C virus -- HCC hepatocellular carcinoma -- KLH keyhole limpet hemocyanin -- r recombinant -- PIDC pre-immune DC -- GFP green fluorescent protein -- UTMD microbubble destruction -- MI mechanic index -- TGE transient gene expression -- EGE extended gene expression -- VLP virus-like particles; Human papillomavirus -- E7 oncoprotein -- Dendritic cell -- Mesenchymal stem cell -- Small heat shock protein; Immunochemistry -- Periodicals; Molecular biology -- Periodicals; Immunochemistry -- Periodicals; Allergy and Immunology -- Periodicals; Molecular Biology -- Periodicals; Immunochimie -- Périodiques; Biologie moléculaire -- Périodiques; Immunochemistry; Molecular biology; Periodicals; Electronic journals; 571.96
• DOI: 10.1016/j.molimm.2019.02.016
• Languages: English
• ISSNs: 0161-5890

Abstract

Highlights: DCs are strong APCs which prime in vitro and in vivo T-cell activities. Potent gene delivery is a major key for using MSCs in tissue engineering. MSCs can develop anticancer therapeutic or antimicrobial prophylactic vaccines. DC and MSC vaccinations are effective for immunotherapy against HPV infections. Abstract: Immunotherapy with DCs as antigen-presenting vehicles have already improved patients' outcome against a variety of tumors. Moreover, MSCs were recently used to develop anti-cancer therapeutic or anti-microbial prophylactic vaccines. The current study evaluated immune responses and anti-tumor effects generated by DCs and MSCs derived from mouse bone marrow which were modified with small heat shock proteins 27 and 20 (sHsp27 and sHsp20) and also E7 oncoprotein in tumor mouse model. Two vaccination strategies were utilized including homologous DC or MSC prime/ DC or MSC boost, and heterologous MSC or DC prime/ protein boost vaccinations. Our data revealed that DCs pulsed with E7+Hsp27 and/or E7+Hsp20 in homologous and heterologous prime/ boost vaccinations could stimulate high levels of IgG2a, IgG2b, IFN-γ and IL-10 directed toward Th1 responses. Moreover, these regimens induced an increased level of Granzyme B, and displayed complete protection more than 60 days after treatment. On the other hand, MSCs transfected with E7+Hsp27 DNA in homologous and heterologous prime/ boost vaccinations could significantly enhance the E7-specific T-cell responses and suppress tumor growth in mice. However, MSCs transfected with E7+Hsp20 DNA did not induce a complete protection against TC-1 tumor compared to DCs pulsed with E7+Hsp20 protein complexes. These results indicated that DC- and MSC-based vaccinations with specific modalities will be a useful approach for immunotherapy and protection against HPV-associated cancers.