HIV infection and specific mucosal immunity: workshop 4B
- PMID: 21441496
- PMCID: PMC11506872
- DOI: 10.1177/0022034511400222
HIV infection and specific mucosal immunity: workshop 4B
Abstract
Most HIV infections are transmitted across mucosal epithelium. An area of fundamental importance is understanding the role of innate and specific mucosal immunity in susceptibility or protection against HIV infection, as well as the effect of HIV infection on mucosal immunity, which leads to increased susceptibility to bacterial, fungal, and viral infections of oral and other mucosae. This workshop attempted to address 5 basic issues-namely, HIV acquisition across mucosal surfaces, innate and adaptive immunity in HIV resistance, antiviral activity of breast milk as a model mucosal fluid, neutralizing immunoglobulin A antibodies against HIV, and progress toward a mucosal vaccine against HIV. The workshop attendants agreed that progress had been made in each area covered, with much recent information. However, these advances revealed how little work had been performed on stratified squamous epithelium compared with columnar epithelium, and the attendants identified several important biological questions that had not been addressed. It is increasingly clear that innate immunity has an important biological role, although basic understanding of the mechanisms of normal homeostasis is still being investigated. Application of the emerging knowledge was lacking with regard to homeostatic mucosal immunity to HIV and its role in changing this homeostasis. With regard to breast milk, a series of studies have demonstrated the differences between transmitters and nontransmitters, although whether these findings could be generalized to other secretions such as saliva was less clear. Important progress toward an oral mucosal HIV vaccine has been made, demonstrating proof of principle for administering vaccine candidates into oral lymphoid tissues to trigger anti-HIV local and systemic immune responses. Similarly, experimental data emphasized the central role of neutralizing antibodies to prevent HIV infection via mucosal routes.
Figures
Similar articles
-
The effects of HIV infection on oral mucosal immunity.Adv Dent Res. 2006 Apr 1;19(1):29-35. doi: 10.1177/154407370601900107. Adv Dent Res. 2006. PMID: 16672546 Review.
-
Broadly Neutralizing Antibodies Display Potential for Prevention of HIV-1 Infection of Mucosal Tissue Superior to That of Nonneutralizing Antibodies.J Virol. 2016 Dec 16;91(1):e01762-16. doi: 10.1128/JVI.01762-16. Print 2017 Jan 1. J Virol. 2016. PMID: 27795431 Free PMC article.
-
Oral mucosal immunity and HIV infection: current status.Oral Dis. 2002;8 Suppl 2:55-62. doi: 10.1034/j.1601-0825.2002.00013.x. Oral Dis. 2002. PMID: 12164661 Review.
-
Association of HIV-1 Envelope-Specific Breast Milk IgA Responses with Reduced Risk of Postnatal Mother-to-Child Transmission of HIV-1.J Virol. 2015 Oct;89(19):9952-61. doi: 10.1128/JVI.01560-15. Epub 2015 Jul 22. J Virol. 2015. PMID: 26202232 Free PMC article. Clinical Trial.
-
Predominate HIV1-specific IgG activity in various mucosal compartments of HIV1-infected individuals.Clin Immunol. 2000 Oct;97(1):59-68. doi: 10.1006/clim.2000.4910. Clin Immunol. 2000. PMID: 10998318
Cited by
-
Oral innate immunity in HIV infection in HAART era.J Oral Pathol Med. 2016 Jan;45(1):3-8. doi: 10.1111/jop.12304. Epub 2015 Jan 31. J Oral Pathol Med. 2016. PMID: 25639844 Free PMC article. Review.
References
-
- Asakura Y, Lundholm P, Kjerrström A, Benthin R, Lucht E, Fukushima J, et al. . (1999). DNA-plasmids of HIV-1 induce systemic and mucosal immune responses. Biol Chem 380:375-379. - PubMed
-
- Bomsel M, David V. (2002). Mucosal gatekeepers: selecting HIV viruses for early infection. Nat Med 8:114-116. - PubMed
-
- Bukawa H, Sekigawa K, Hamajima K, Fukushima J, Yamada Y, Kiyono H, et al. . (1995). Neutralization of HIV-1 by secretory IgA induced by oral immunization with a new macromolecular multicomponent peptide vaccine candidate. Nat Med 1:681-685. - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical