2002
DOI: 10.1016/s0165-2427(02)00033-8
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Recruitment of intestinal CD45RA+ and CD45RC+ cells induced by a candidate oral vaccine against porcine post-weaning colibacillosis

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Cited by 20 publications
(18 citation statements)
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“…Such immunostimulatory effects of the copolymers on Th1 and Th2 responses following the facilitation of uptake of exogenous antigens by APC have been reported [13]. The diversity of the immune cell subsets that could be stimulated by POE-POP in the postweanling pig model system, it suggests that the copolymers when applied as the adjuvant with specific vaccinal immunogen (non-ETEC strain) or alone as an IRM (applied in the current study), may affect either the immunologically commited (T, B and NK-cells) or naïve (CD45RA + ) lymphoid cells [29]. Consistent with a former finding of selectively activated CD1 + and CD21 + gut-residing B cells is our previous finding of stimulated proliferation of IgA + plasma cells and sIgA antibodies by the immunization with POE-POP adjuvanted non-ETEC vaccine candidate strain [20,32].…”
Section: Discussionmentioning
confidence: 88%
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“…Such immunostimulatory effects of the copolymers on Th1 and Th2 responses following the facilitation of uptake of exogenous antigens by APC have been reported [13]. The diversity of the immune cell subsets that could be stimulated by POE-POP in the postweanling pig model system, it suggests that the copolymers when applied as the adjuvant with specific vaccinal immunogen (non-ETEC strain) or alone as an IRM (applied in the current study), may affect either the immunologically commited (T, B and NK-cells) or naïve (CD45RA + ) lymphoid cells [29]. Consistent with a former finding of selectively activated CD1 + and CD21 + gut-residing B cells is our previous finding of stimulated proliferation of IgA + plasma cells and sIgA antibodies by the immunization with POE-POP adjuvanted non-ETEC vaccine candidate strain [20,32].…”
Section: Discussionmentioning
confidence: 88%
“…A single cell suspensions (100 μL) were prepared in triplicates (comprising 10,000 cells each) and incubated with mAbs (50 μL) (Table  1) and processed as described previously [29]. The fluorescence of the mAb-labelled porcine lymphoid cells was quantified using a Coulter EPICS-XL flow cytometer (Beckman Coulter, Miami, FL, USA) as detailed earlier [30].…”
Section: Methodsmentioning
confidence: 99%
“…One million passage 3 ASCs were suspended in 100 μL PBS containing 10 μg/ml fluorescein isothiocyanate-conjugated primary antibodies specific to mesenchymal stromal cells (MSCs) (CD29, CD44, CD90, and CD105) and hematopoietic cells (CD31 and CD45) (n = 3). The following expression markers reactive with the porcine antigen isoforms were used: Alexa Fluor 647 Mouse Anti-Pig CD29 (BD Bioscience, New Jersey, USA), Anti-CD44 antibody [IM7] (Abcam plc, Cambridge, UK), APC Mouse Anti-Human CD90 (BD-Biosciences), Anti-CD105 antibody [MEM-229] (Abcam plc), PE Mouse Anti-Rat CD31 (BD Biosciences), and Monoclonal Antibody to CD45/LCA (CD45R)-PE (Acris Antibodies, Inc. CA, USA) [24] , [25] , [26] , [27] , [28] . Cell fluorescence was evaluated with a Gallios flow cytometer (Beckman Coulter, Tokyo, Japan) and the data were analyzed using Karuza for Gallios software (Beckman Coulter).…”
Section: Methodsmentioning
confidence: 99%
“…Blood samples (1 ml) from 7 pigs in each group were taken weekly from vena cava cranialis into glass tubes (Beckton Dickinson, Plymouth, UK) with ethylenediaminetetraacetic acid (EDTA) (Sigma, Germany) as anticoagulant for FCM analysis as described previously (Valpotić et al 1994;Božić et al 2002).…”
Section: Bacteriologymentioning
confidence: 99%