2018
DOI: 10.3390/vaccines6040084
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T Cell Memory to Vaccination

Abstract: Most immune responses associated with vaccination are controlled by specific T cells of a CD4+ helper phenotype which mediate the generation of effector antibodies, cytotoxic T lymphocytes (CTLs), or the activation of innate immune effector cells. A rapidly growing understanding of the generation, maintenance, activity, and measurement of such T cells is leading to vaccination strategies with greater efficacy and potentially greater microbial coverage.

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Cited by 26 publications
(25 citation statements)
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“…Subunit vaccines often suffer from poor immunogenicity and require certain helper molecules known as adjuvants to induce or enhance an appropriate immune response to the antigen. T‐cell activation is crucial in inducing protective immune responses (Todryk, 2018). Antigens mannosylated by P. pastoris have shown to have enhanced antigen presentation and T‐cell activation properties compared with their nonglycosylated counterparts.…”
Section: The Characteristic Features Of P Pastoris Expression Systemmentioning
confidence: 99%
“…Subunit vaccines often suffer from poor immunogenicity and require certain helper molecules known as adjuvants to induce or enhance an appropriate immune response to the antigen. T‐cell activation is crucial in inducing protective immune responses (Todryk, 2018). Antigens mannosylated by P. pastoris have shown to have enhanced antigen presentation and T‐cell activation properties compared with their nonglycosylated counterparts.…”
Section: The Characteristic Features Of P Pastoris Expression Systemmentioning
confidence: 99%
“…Upon exposure to that pathogen at some time in the future, long‐lived memory cells awaken and recognize the antigen against which they were generated and mount a pathogen‐specific response, resulting in protection against the infection and associated disease. [ 15,16 ]…”
Section: Vaccination and Immunological Memorymentioning
confidence: 99%
“…A subset of these T and B cells, in turn, differentiates into long‐lived memory cells that are able to respond almost immediately upon re‐exposure to that antigen, bypassing the need for a de novo response. [ 15–20 ] It is, therefore, necessary for vaccine formulations to be designed with different combinations of antigens to promote protective immunity through strong initial interactions with APCs.…”
Section: Vaccination and Immunological Memorymentioning
confidence: 99%
“…For the evaluation of immune response, we performed four immunizations (on days 1, 14, 28, and 42). This scheme had an extra booster compared to the scheme described below, which was used in order to enable the generation of a supposed "protective" level of effector T cells [31]. This model ended on day 43, when the animals were euthanized to obtain the genitouterine tract, blood, spleen, and small intestine.…”
Section: Oral Immunization and Gbs Vaginal Colonizationmentioning
confidence: 99%