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. Author manuscript; available in PMC: 2013 Feb 25.
Published in final edited form as: Vet Immunol Immunopathol. 2008 Jan 20;123(1-2):65–80. doi: 10.1016/j.vetimm.2008.01.030

Table 5.

Vaccine-induced T-cell immunity important in protection observed in adoptive-transfer (A-T) studies

Study-Group A-T Donor Cats
A-T Donor-Recipient Matching
Number of Recipients FIV Statusc Protection Rate (%)
Immune Status Cell Typea MLR MHC-I b MHC-II b
F2 generation against homologous FIVPet challenge
1A Vaccinate T cell Matched ND ND 3 3 / 4 (75%)
Vaccinate T cell Matched ND ND 1 +
1B Vaccinate B cell Matched ND ND 2 + 0 / 2 ( 0% )
1C Non-vaccinate PBMC Unmatched ND ND 2 + 0 / 2 ( 0% )
F3/F4 generations against homologous FIVPet challenge
2A Vaccinate T cell Matched Identical ND 4 4 / 4 (100%)
2B Vaccinate CD8+ T cell Matched Identical ND 2 2 / 3 (67%)
Vaccinate CD8+ T cell Matched None ND 1 +
2C Vaccinate CD4+ T cell Matched Identicald ND 2 2 / 3 (67%)
Vaccinate CD4+ T cell Matched Identical None 1 +
2D Non-vaccinate T cell Matched ND ND 1 + 0 / 2 ( 0% )
Non-vaccinate PBMC Unmatched ND ND 1 +
2E None PBS None NA NA 2 + 0 / 2 ( 0% )
F3/F4 generations against heterologous-subtype-B FIVFC1 challenge
3A Vaccinate T cell Matched ND ND 2 2 / 4 (50%)
Vaccinate T cell Matched ND ND 2 +
3B Vaccinate T cell Unmatched ND ND 2 + 0 / 2 ( 0% )
3C None PBS None NA NA 4 + 0 / 4 ( 0% )
a

Cell type from donor cat adoptively transferred to recipient cat. PBMC were purified by magnetic cell separation systems of Miltenyi Biotec, Inc. (Auburn, CA) in Study 1 and R&D Systems (Minneapolis, MN) in Studies 2 and 3.

b

Not done (ND); not applicable (NA); >37% of the MHC sequences were identical (Identical); none or <10% of the MHC sequences were identical (none).

c

FIV status (+ or −) after challenge with either homologous strain (Studies 1 & 2) or heterologous-subtype-B strain (Study 3).

d

One pair was not tested but the other pair had >50% of identical MHC-I sequences.