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Streptococcal Immunity Is Constrained by Lack of Immunological Memory following a Single Episode of Pyoderma.

ABSTRACT: The immunobiology underlying the slow acquisition of skin immunity to group A streptococci (GAS), is not understood, but attributed to specific virulence factors impeding innate immunity and significant antigenic diversity of the type-specific M-protein, hindering acquired immunity. We used a number of epidemiologically distinct GAS strains to model the development of acquired immunity. We show that infection leads to antibody responses to the serotype-specific determinants on the M-protein and profound protective immunity; however, memory B cells do not develop and immunity is rapidly lost. Furthermore, antibodies do not develop to a conserved M-protein epitope that is able to induce immunity following vaccination. However, if re-infected with the same strain within three weeks, enduring immunity and memory B-cells (MBCs) to type-specific epitopes do develop. Such MBCs can adoptively transfer protection to naïve recipients. Thus, highly protective M-protein-specific MBCs may never develop following a single episode of pyoderma, contributing to the slow acquisition of immunity and to streptococcal endemicity in at-risk populations.

SUBMITTER: Pandey M 

PROVIDER: S-EPMC5222516 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Streptococcal Immunity Is Constrained by Lack of Immunological Memory following a Single Episode of Pyoderma.

Pandey Manisha M   Ozberk Victoria V   Calcutt Ainslie A   Langshaw Emma E   Powell Jessica J   Rivera-Hernandez Tania T   Ho Mei-Fong MF   Philips Zachary Z   Batzloff Michael R MR   Good Michael F MF  

PLoS pathogens 20161227 12

The immunobiology underlying the slow acquisition of skin immunity to group A streptococci (GAS), is not understood, but attributed to specific virulence factors impeding innate immunity and significant antigenic diversity of the type-specific M-protein, hindering acquired immunity. We used a number of epidemiologically distinct GAS strains to model the development of acquired immunity. We show that infection leads to antibody responses to the serotype-specific determinants on the M-protein and  ...[more]