T-cell-inducing vaccines - what's the future

被引:128
作者
Gilbert, Sarah C. [1 ]
机构
[1] Univ Oxford, Jenner Inst, Oxford OX3 7DQ, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
adjuvants; clinical trials; T cell; vaccine; viral vectored vaccines; TEST-OF-CONCEPT; VIRUS ANKARA; CIRCUMSPOROZOITE PROTEIN; NEUTRALIZING ANTIBODIES; HIV-1; VACCINE; ME-TRAP; MEDIATED PROTECTION; IMMUNE-RESPONSES; MALARIA VACCINE; VIRAL VECTORS;
D O I
10.1111/j.1365-2567.2011.03517.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the twentieth century vaccine development has moved from the use of attenuated or killed micro-organisms to protein sub-unit vaccines, with vaccine immunogenicity assessed by measuring antibodies induced by vaccination. However, for many infectious diseases T cells are an important part of naturally acquired protective immune responses, and inducing these by vaccination has been the aim of much research. The progress that has been made in developing effective T-cell-inducing vaccines against viral and parasitic diseases such as HIV and malaria is discussed, along with recent developments in therapeutic vaccine development for chronic viral infections and cancer. Although many ways of inducing T cells by vaccination have been assessed, the majority result in low level, non-protective responses. Sufficient clinical research has now been conducted to establish that replication-deficient viral vectored vaccines lead the field in inducing strong and broad responses, and efficacy studies of T-cell-inducing vaccines against a number of diseases are finally demonstrating that this is a valid approach to filling the gaps in our defence against not only infectious disease, but some forms of cancer.
引用
收藏
页码:19 / 26
页数:8
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