1999
DOI: 10.1016/s0165-2427(99)00065-3
|View full text |Cite
|
Sign up to set email alerts
|

Long term substitution and specific immune responses after transfer of bovine peripheral blood lymphocytes into severe combined immunodeficient mice

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2006
2006
2011
2011

Publication Types

Select...
2
1

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 43 publications
0
1
0
Order By: Relevance
“…Immunostaining with an anti-CD4 antibody did not reveal significant differences between tumors obtained from the different experimental groups (Supplementary Figure S7i), suggesting that the population of lymphocytes infiltrating the tumors is largely NK cells and CD8 + cytotoxic T cells. CD8 + cytotoxic T lymphocyte (CTL)-dependent immunity is known to contribute to the PBL-dependent suppression of tumor xenografts in hu-PBL-NOD/SCID mouse models. The CTL immune response might also be expected to be high in LNCaP tumor cells treated with ligand 1 that are dying by ADCC, since this mechanism of cytotoxicity can enhance tumor cell immunogenicity . Previous reports suggest that a considerable fraction of the PBL injected into SCID mice might be specific to the host antigens.…”
Section: Resultsmentioning
confidence: 99%
“…Immunostaining with an anti-CD4 antibody did not reveal significant differences between tumors obtained from the different experimental groups (Supplementary Figure S7i), suggesting that the population of lymphocytes infiltrating the tumors is largely NK cells and CD8 + cytotoxic T cells. CD8 + cytotoxic T lymphocyte (CTL)-dependent immunity is known to contribute to the PBL-dependent suppression of tumor xenografts in hu-PBL-NOD/SCID mouse models. The CTL immune response might also be expected to be high in LNCaP tumor cells treated with ligand 1 that are dying by ADCC, since this mechanism of cytotoxicity can enhance tumor cell immunogenicity . Previous reports suggest that a considerable fraction of the PBL injected into SCID mice might be specific to the host antigens.…”
Section: Resultsmentioning
confidence: 99%