Maternal antibodies inhibit neonatal and infant responses to vaccination by shaping the early-life B cell repertoire within germinal centers

Autor: Christiane S. Eberhardt, Paul-Henri Lambert, Maria Vono, Sylvain Lemeille, Dennis Christensen, Beatris Mastelic-Gavillet, Claire-Anne Siegrist, Floriane Auderset, Peter Andersen
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
Male
Antibody Formation/immunology
T-Lymphocytes
ddc:616.07
Antibodies
Viral

Inbred C57BL
Mice
0302 clinical medicine
Orthomyxoviridae Infections/immunology/virology
Pregnancy
germinal centers
Gene expression
Maternal-Fetal Exchange
lcsh:QH301-705.5
Inbred BALB C
B-Lymphocytes
Mice
Inbred BALB C

Orthomyxoviridae/immunology
biology
Helper-Inducer/immunology
Vaccination
repertoire
B-Lymphocytes/immunology
T-Lymphocytes
Helper-Inducer

Orthomyxoviridae
3. Good health
Antibodies/blood/immunology
epitope masking
medicine.anatomical_structure
Female
Antibody
Offspring
General Biochemistry
Genetics and Molecular Biology

Antibodies
03 medical and health sciences
Germinal Center/immunology
Orthomyxoviridae Infections
medicine
Animals
Gene
B cell
Germinal center
Maternal-Fetal Exchange/immunology
Germinal Center
Newborn
neonates
Mice
Inbred C57BL

030104 developmental biology
maternal antibodies
Immunoglobulin class switching
Immunization
Animals
Newborn

lcsh:Biology (General)
Immunology
Antibody Formation
biology.protein
Viral/blood/immunology
030217 neurology & neurosurgery
Zdroj: Cell Reports, Vol. 28, No 7 (2019) pp. 1773-1784.e5
Vono, M, Eberhardt, C S, Auderset, F, Mastelic-Gavillet, B, Lemeille, S, Christensen, D, Andersen, P, Lambert, P H & Siegrist, C A 2019, ' Maternal Antibodies Inhibit Neonatal and Infant Responses to Vaccination by Shaping the Early-Life B Cell Repertoire within Germinal Centers ', Cell Reports, vol. 28, no. 7, pp. 1773-1784.e5 . https://doi.org/10.1016/j.celrep.2019.07.047
Cell Reports, Vol 28, Iss 7, Pp 1773-1784.e5 (2019)
ISSN: 2211-1247
DOI: 10.1016/j.celrep.2019.07.047
Popis: Summary: Maternal antibodies (MatAbs) protect offspring from infections but limit their responses to vaccination. The mechanisms of this inhibition are still debated. Using murine early-life immunization models mimicking the condition prevailing in humans, we observed the induction of CD4-T, T follicular helper, and germinal center (GC) B cell responses even when early-life antibody responses were abrogated by MatAbs. GC B cells induced in the presence of MatAbs form GC structures and exhibit canonical GC changes in gene expression but fail to differentiate into plasma cells and/or memory B cells in a MatAb titer-dependent manner. Furthermore, GC B cells elicited in the presence or absence of MatAbs use different VH and Vk genes and show differences in genes associated with B cell differentiation and isotype switching. Thus, MatAbs do not prevent B cell activation but control the output of the GC reaction both quantitatively and qualitatively, shaping the antigen-specific B cell repertoire. : Maternal antibodies (MatAbs) protect offspring from infections but limit their vaccine responses through still poorly known mechanisms. Vono et al. report that MatAbs do not prevent B cell activation or germinal center formation but control plasma cell and memory B cell differentiation, shaping the long-term antigen-specific B cell repertoire. Keywords: immunization, maternal antibodies, neonates, repertoire, germinal centers, epitope masking
Databáze: OpenAIRE