» Articles » PMID: 19201877

Absence of Mucosal Immunity in the Human Upper Respiratory Tract to the Commensal Bacteria Neisseria Lactamica but Not Pathogenic Neisseria Meningitidis During the Peak Age of Nasopharyngeal Carriage

Overview
Journal J Immunol
Date 2009 Feb 10
PMID 19201877
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The normal flora that colonizes the mucosal epithelia has evolved diverse strategies to evade, modulate, or suppress the immune system and avoid clearance. Neisseria lactamica and Neisseria meningitidis are closely related obligate inhabitants of the human upper respiratory tract. N. lactamica is a commensal but N. meningitidis is an opportunistic pathogen that occasionally causes invasive disease such as meningitis and septicemia. We demonstrate that unlike N. meningitidis, N. lactamica does not prime the development of mucosal T or B cell memory during the peak period of colonization. This cannot be explained by the induction of peripheral tolerance or regulatory CD4(+)CD25(+) T cell activity. Instead, N. lactamica mediates a B cell-dependent mitogenic proliferative response that is absent to N. meningitidis. This mitogenic response is associated with the production of T cell-independent polyclonal IgM that we propose functions by shielding colonizing N. lactamica from the adaptive immune system, maintaining immunological ignorance in the host. We conclude that, in contrast to N. meningitidis, N. lactamica maintains a commensal relationship with the host in the absence of an adaptive immune response. This may prolong the period of susceptibility to colonization by both pathogenic and nonpathogenic Neisseria species.

Citing Articles

Commensal Neisseria species share immune suppressive mechanisms with Neisseria gonorrhoeae.

Zhu W, Cardenas-Alvarez M, Tomberg J, Little M, Duncan J, Nicholas R PLoS One. 2023; 18(4):e0284062.

PMID: 37027389 PMC: 10081783. DOI: 10.1371/journal.pone.0284062.


Outer Membrane Vesicles: An Emerging Vaccine Platform.

Kashyap D, Panda M, Baral B, Varshney N, R S, Bhandari V Vaccines (Basel). 2022; 10(10).

PMID: 36298443 PMC: 9610665. DOI: 10.3390/vaccines10101578.


Exploring the Ability of Meningococcal Vaccines to Elicit Mucosal Immunity: Insights from Humans and Mice.

Currie E, Gray-Owen S Pathogens. 2021; 10(7).

PMID: 34358056 PMC: 8308890. DOI: 10.3390/pathogens10070906.


A recombinant commensal bacteria elicits heterologous antigen-specific immune responses during pharyngeal carriage.

Laver J, Gbesemete D, Dale A, Pounce Z, Webb C, Roche E Sci Transl Med. 2021; 13(601).

PMID: 34233953 PMC: 7615050. DOI: 10.1126/scitranslmed.abe8573.


Innate and adaptive nasal mucosal immune responses following experimental human pneumococcal colonization.

Jochems S, de Ruiter K, Solorzano C, Voskamp A, Mitsi E, Nikolaou E J Clin Invest. 2019; 129(10):4523-4538.

PMID: 31361601 PMC: 6763269. DOI: 10.1172/JCI128865.