Immune responses induced by BCG recombinant for human papillomavirus L1 and E7 proteins


Autoria(s): Abdul Jabbar, I.; Fernando, G. J.; Saunders, N. A.; Aldovini, A.; Young, R.; Malcolm, K. M.; Frazer, I. H.
Data(s)

01/05/2000

Resumo

Recombinant bacille Calmette-Guerin (BCG) based vaccine delivery systems could potentially share the safety and effectiveness of BCG. We therefore prepared recombinant BCG vaccines which expressed the L1 late protein of the human papillomavirus (HPV) 6b or the E7 early protein of the HPV 16. The two recombinants were evaluated as immunogens in C57BL/6J and BALB/c mice, and compared with a conventional protein/adjuvant system using E7 or L1 mixed with Quil-A adjuvant. rBCG6bL1 and rBCG16E7 primed specific immune responses, represented by DTH, T-proliferation and antibody, and rBCG16E7 induced cytotoxic immune response to E7 protein. The magnitude of the observed responses were less than those elicited by protein/adjuvant vaccine. As recombinant BCG vaccines expressing HPV6bL1 or HPV16E7 persist at low levels in the immunised host, they may be beneficial to prime or retain memory responses to antigens, but are unlikely to be useful as a single component vaccine strategy. (C) 2000 Elsevier science Ltd. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:36384

Idioma(s)

eng

Publicador

Elsevier

Palavras-Chave #Immunology #Medicine, Research & Experimental #Veterinary Sciences #Calmette-guerin #Transforming Protein #Protective Immunity #Foreign Antigen #Type-16 #Mice #Immunization #Vaccine #Epitopes #Cells #C1 #320299 Immunology not elsewhere classified #730101 Infectious diseases
Tipo

Journal Article