Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-89wxm Total loading time: 0 Render date: 2024-07-07T18:16:21.312Z Has data issue: false hasContentIssue false

8 - Cellular immunity in HIV: a synthesis of responses to preserve self

Published online by Cambridge University Press:  07 September 2011

Clive Gray
Affiliation:
Stanford University
Netty Malatsi
Affiliation:
University of Johannesburg
Catherine Riou
Affiliation:
University Claude Bernard
Debra de Assis Rosa
Affiliation:
Nicd Aids Unit in Johannesburg
S. S. Abdool Karim
Affiliation:
University of KwaZulu-Natal, South Africa
Q. Abdool Karim
Affiliation:
University of KwaZulu-Natal, South Africa
Get access

Summary

IN THIS CHAPTER SALIENT points are brought into focus concerning general immunity and immunity to HIV-1 infection. An effective and efficient immune response develops to preserve self from non-self and a discriminating recognition process has evolved to ensure this. HIV-1 has successfully undermined the discriminating process and leaves the infected host open to many diseases where there is no longer an ability to preserve self. However, some HIV-1 infected individuals do not progress to AIDS and others appear to be resistant to infection. These individuals are thought to mount highly effective immune responses that provide some form of protection. The objective of many research efforts has been and will be to determine what type of immunity these individuals develop.

There are already some clues that certain host genes, such as hla backgrounds, are important and that strong T-cell immunity develops in people who progress slowly. Additionally, it is thought that events in the first few months of hiv-1 infection are crucial to emulate with a vaccine – as it is the T-cell responses to recently transmitted viruses that are the most effective at controlling viral replication. It is likely that the most important point at which pathogenesis takes hold and there is a ‘point of no return’, is when hiv-1 seeds to the lymphoid depots and begins to precipitate lymphoid structure degeneration. At this point, drug intervention is the only mechanism that would allow the immune system to restore, as drug-induced viral suppression would allow lymphoid structures to regenerate.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×