Author: Sakala, Isaac G.; Eichinger, Katherine Marie; Petrovsky, Nikolai
Title: Neonatal vaccine effectiveness and the role of adjuvants Cord-id: g9ev443o Document date: 2019_7_25
ID: g9ev443o
Snippet: Introduction: Neonates are less responsive to vaccines than adults, making it harder to protect newborns against infection. Neonatal differences in antigen-presenting cell, B and T cell function, all likely contribute. A key question is whether novel adjuvants might be able to make neonatal vaccines more effective. Areas covered: This review addresses the issues of how to improve neonatal vaccines, which we have defined as vaccines given in the first 4 weeks of life in a human infant or the firs
Document: Introduction: Neonates are less responsive to vaccines than adults, making it harder to protect newborns against infection. Neonatal differences in antigen-presenting cell, B and T cell function, all likely contribute. A key question is whether novel adjuvants might be able to make neonatal vaccines more effective. Areas covered: This review addresses the issues of how to improve neonatal vaccines, which we have defined as vaccines given in the first 4 weeks of life in a human infant or the first week of life in a mouse. A search was performed using keywords including ‘neonatal immunity’, ‘neonatal immunisation’, ‘vaccine’ and ‘adjuvant’ of PubMed articles published between 1960 and 2018. Expert opinion: Sugar-like structures have recently been shown to prime the infant adaptive immune system to respond to vaccines, being potentially more effective than traditional adjuvants. Sugar-based compounds with beneficial adjuvant effects in neonatal vaccine models include delta inulin (Advax), curdlan, and trehalose 6,6ʹ-dibehenate. Such compounds make interesting neonatal adjuvant candidates, either used alone or in combination with traditional innate immune adjuvants.
Search related documents:
Co phrase search for related documents- acute infection and adaptive immune system: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17
- acute infection and adaptive immunity: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36
- acute infection and additional research: 1, 2, 3, 4, 5
- acute infection and adjuvant benefit: 1
- acute infection and adjuvant combination: 1, 2
- acute infection and adjuvant safety: 1, 2
- acute infection and low antibody: 1, 2, 3, 4, 5, 6, 7
- acute infection and low expression: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14
- acute infection and low level immunity: 1
- acute infection and low respiratory infection: 1, 2, 3, 4, 5, 6, 7, 8
- acute infection and low response: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13
- acute infection and lung pathology: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24
- acute infection and lymph node: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14
- adaptive immune response and additional research: 1
- adaptive immune response and adjuvant activity: 1, 2, 3, 4
- adaptive immune response and adjuvant effect: 1, 2
- adaptive immune response and adjuvant formulation: 1, 2, 3
- adaptive immune response and lung pathology: 1, 2, 3, 4
- adaptive immune response and lymph node: 1, 2, 3, 4, 5, 6
Co phrase search for related documents, hyperlinks ordered by date