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. 2003 Feb;108(2):129–136. doi: 10.1046/j.1365-2567.2003.01568.x

Table 1.

Inhibition of plaque development in syngeneic monolayer by different types of rat lymph node-derived cell populations

No of plaques (Mean ± SD) PFU/ml in culture fluid


Type of cells* Days after infection Day 4 Day 7 Day 8 Day 10 Day 12
1. Infected monolayer only 47·0 ± 3·7 > 200 Confluent Confluent 64000
2. PLNc, γδ T+ 2 7·0 ± 2·6 19·7 ± 2·5 > 20d Confluent 68000
3. PLNi, γδ T+ 2 2·5 ± 1·3 9·3 ± 1·5 9·3 ± 1·5 9·3 ± 1·5 3000
4. PLNi, γδ T 2 8·3 ± 0·96 51·0 ± 6·6 Confluent Confluent 52000
5. PLNi, CD8+ 6 1·3 ± 0·96 0·3 ± 0·5 0·3 ± 0·5 0 0
6. PLNi, γδ T 6 4·5 ± 1·3 4·0 ± 0·8 3·3 ± 1·0 3·3 ± 1·0§ 0
7. PLNi, γδ T+ 6 0 2·3 ± 1·9 2·3 ± 1·9 2·3 ± 1·9§ 0
8. PLNi, γδ T+ (NKR-PI depleted) 6 4·8 ± 1·7 4·3 ± 1·0 4·3 ± 0·96 1·8 ± 0·9 0
9. PLNi, γδ T+(NKR-PI depleted)anti-IFN-γ 6 29·3 ± 4·6 > 200 Confluent Confluent 64000
*

A total of 50 000 γδ T+ or γδ T cell fractions, as well as CD8+ cells, were plated on syngeneic fibroblast monolayers (10 000 fibroblasts/well) preinfected 2 hr previously with 50 plaque-forming units (PFU) of aMCMV [Smith's strain murine cytomegalovirus (MCMV), passaged three or four times through the rat fibroblast monolayer] in 0·1 ml of Dulbecco's modified Eagle's minimal essential medium (DMEM); in rows 8 and 9 the negative selected γδ T cells depleted from NKR-P1+ were used. PLNc, contralateral popliteal lymph nodes; PLNi, draining popliteal lymph nodes.

DA rats were injected with 10 000 PFU of aMCMV into the footpad; PLN cells were derived either day 2 or day 6 after inoculation with aMCMV.

Plaques were dramatically enlarged in size.

§

Plaques were arrested.

IFN-γ, interferon-γ.