Sentence examples for cellular immunization from inspiring English sources

To circumvent the embryo-lethality of ABP1 knock-out [7], we used ethanol inducible conditional knock-down plants generated via an antisense ABP1 construct to decrease its expression (ABP1AS lines) or via cellular immunization to inactivate ABP1 protein through its in vivo interaction with the recombinant antibody scFv12.

Four mice from the vaccinated group were sacrificed on 7th day after the fifth immunization, and cellular immune responses were analyzed.

These results indicated that the R848 and poly(I C) together with Al(OH 3 enhanced humoral and cellular immune responses to immunization with 146S FMDV antigens.

In contrast to passive antibody administration, most efforts to examine cellular immunity involve direct immunization of mice, which examines: the antigen; the mode of delivery; and the immunogenicity of the antigen, including presentation by both class I and class II MHC molecules.

A slight increase in the release of IL-4 (as well as IgG1) in combination with the high levels of IL-2 and IFN-γ suggested the activation of an appropriate T helper response, primarily a specific Th1-biased cellular immune response after immunization with CAV-2-ROP18.

After immunization, humoral and cellular immune responses were detected by ELISA and flow cytometry.

In this study, we examine both humoral and cellular immune responses elicited by immunization with peptide or DNA encoding wild-type and the Flemish and Dutch mutations of ABeta42 (i.e. the beta amyloid peptide spanning amino acids 1 42) in mice of different immune haplotypes as well as HLA Class II transgenic mice.

In order to assess the cellular immune responses generated after immunization we performed an in vitro re-stimulation of splenocytes from vaccinated mice with Class I and II H-2d restricted hemagglutinin (HA) or nucleoprotein (NP) peptides.

The humoral and cellular immune responses upon peptide immunization were analyzed by ELISA and multiparameter flow cytometry, respectively.

Two separate cohorts were used for the evaluation of in vitro cellular immune responses 2 weeks after the 3d immunization dose immunization and for the duration of the humoral responses 12 weeks after the completion of the vaccination regimen.

The antibody titers and cellular immune responses were assayed after immunization.