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Cited by 593

The DOI matches its Crossref record; 110 of the 110 references it cites were found in a registry or an index.

Neonatal and early life vaccinology

Open access
Siegrist, Claire-Anne·2001·Vaccine

Abstract

Preclinical and human vaccine studies indicate that, although neonatal immunisation does not generally lead to rapid and strong antibody responses, it may result in an efficient immunological priming, which can serve as an excellent basis for future responses. The apparent impairment of CD4 and CD8 T-cell function in early life seems to result from suboptimal antigen-presenting cells-T cell interactions, which can be overcome by use of specific adjuvants or delivery systems. Although persistence of maternal antibodies may limit infant antibody responses, induction of T-cell responses largely remain unaffected by these passively transferred antibodies. Thus, neonatal priming and early boosting with vaccine formulations optimised for sufficient early life immunogenicity and maximal safety profiles, could allow better control of the huge infectious disease burden in early life.

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Crossref · 10.1016/s0264-410x(01)00028-7

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Metadata

Authors
Siegrist, C.-A.
Venue
Vaccine
Publisher
Elsevier BV
Published
2001-05
Volume
19
Issue
25-26
Pages
3331-3346
ISSN
0264-410X (ISSN-L)
OpenAlex
W2161291046
Cited by
593
References
110
FWCI
8.83
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Neonatal and early life vaccinology. https://app.cochat.ai/papers/10.1016/s0264-410x(01)00028-7
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Siegrist, C.-A. (2001). Neonatal and early life vaccinology. Vaccine. https://doi.org/10.1016/s0264-410x(01)00028-7

Data sources

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.