2003PubMedRequires access

Cellular immune responses to influenza.

Paul Moss

Open publisher page 21 citations

Abstract

Cellular immune responses are believed to play an important role in controlling influenza infection. CD4+ and CD8+ T cell responses are well described and CD8+ immunity is of paramount importance in killing virally infected cells. In the past few years several novel techniques have been devised which allow quantification of antigen-specific cellular immune responses and these will be reviewed briefly. Influenza-specific cellular immunity is elicited following natural infection and several viral proteins have been identified as targets for cellular responses. Cellular immunity is detectable throughout life in most donors but there is clear evidence of impaired cellular immunity in the elderly, a population at particular risk of influenza infection. This finding must be viewed against the background of 'immune senescence' that is documented with aging. Cellular responses are able to provide heterosubtypic immunity to influenza viral antigens. As such the induction of cellular immune responses is a highly desirable aim of vaccination protocols. Induction of cellular immunity with conventional formalin-inactivated vaccine is poor although some improvement may be derived from novel forms of vaccine delivery such as the use of adjuvanted carriers. Nevertheless, a range of new vaccines is being developed which are more effective in priming cellular responses. Although there is relatively little detail on the nature of the cellular response induced by these agents, they hold out the promise of more effective and durable protection from influenza infection.

About this research paper

What this paper is about

Cellular immune responses are believed to play an important role in controlling influenza infection. CD4+ and CD8+ T cell responses are well described and CD8+ immunity is of paramount importance in killing virally infected cells. In the past few years several novel techniques have been devised which allow quantification of antigen-specific cellular immune responses and these will be reviewed briefly. Influenza-specific cellular immunity is elicited following natural infection and several viral proteins have been identified as targets for cellular responses. Cellular immunity is detectable throughout life in most donors but there is clear evidence of impaired cellular immunity in the elderly, a population at particular risk of influenza infection. This finding must be viewed against the background of 'immune senescence' that is documented with aging. Cellular responses are able to provide heterosubtypic immunity to influenza viral antigens. As such the induction of cellular immune responses is a highly desirable aim of vaccination protocols. Induction of cellular immunity with conventional formalin-inactivated vaccine is poor although some improvement may be derived from novel forms of vaccine delivery such as the use of adjuvanted carriers. Nevertheless, a range of new vaccines is being developed which are more effective in priming cellular responses. Although there is relatively little detail on the nature of the cellular response induced by these agents, they hold out the promise of more effective and durable protection from influenza infection.

Why it matters

OpenAlex reports 21 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Cellular immune responses are believed to play an important role in controlling influenza infection. CD4+ and CD8+ T cell responses are well described and CD8+ immunity is of paramount importance in killing virally infected cells. In the past few years several novel techniques have been devised which allow quantification of antigen-specific cellular immune responses and these will be reviewed briefly. Influenza-specific cellular immunity is elicited following natural infection and several viral proteins have been identified as targets for cellular responses. Cellular immunity is detectable throughout life in most donors but there is clear evidence of impaired cellular immunity in the elderly, a population at particular risk of influenza infection. This finding must be viewed against the background of 'immune senescence' that is documented with aging. Cellular responses are able to provide heterosubtypic immunity to influenza viral antigens. As such the induction of cellular immune responses is a highly desirable aim of vaccination protocols. Induction of cellular immunity with conventional formalin-inactivated vaccine is poor although some improvement may be derived from novel forms of vaccine delivery such as the use of adjuvanted carriers. Nevertheless, a range of new vaccines is being developed which are more effective in priming cellular responses. Although there is relatively little detail on the nature of the cellular response induced by these agents, they hold out the promise of more effective and durable protection from influenza infection.

Key concepts: Cellular immunity, Immune system, Immunology, Immunity, Biology, Vaccination, Antigen, Population

Related papers

Back to paper searchBrowse research topicsOriginal source
Cellular immune responses to influenza. — Research Paper | ScholarLens