Table 1.

Primary LCMV-Specific Effector CTL Response at 8 Days Postinfection

Cell SampleEx Vivo Virus-Specific CTLs (% specific 51Cr release)*
Infected TargetsUninfected TargetsLU
100:130:110:13:1100:130:110:1Per 106 CellsPer 106 CD8+ CellsPer Organ or in Circulation
Spleen ND 82 ± 1 50 ± 6 19 ± 2 ND 3 ± 1  24 ± 8  96 ± 30 2,928 ± 612 
PBMCs 72 69 53 30 25 72 579 
Bone marrow 19 ± 1 8 ± 1 3 ± 1 1 ± 1 0.71 ± 0.08 36 ± 4  162 ± 27 
Cell SampleEx Vivo Virus-Specific CTLs (% specific 51Cr release)*
Infected TargetsUninfected TargetsLU
100:130:110:13:1100:130:110:1Per 106 CellsPer 106 CD8+ CellsPer Organ or in Circulation
Spleen ND 82 ± 1 50 ± 6 19 ± 2 ND 3 ± 1  24 ± 8  96 ± 30 2,928 ± 612 
PBMCs 72 69 53 30 25 72 579 
Bone marrow 19 ± 1 8 ± 1 3 ± 1 1 ± 1 0.71 ± 0.08 36 ± 4  162 ± 27 

Adult BALB/c mice were infected intraperitoneally with 2 × 105 PFU LCMV-Armstrong, and cytolytic virus-specific CTL activity was determined in the spleen, peripheral blood, and bone marrow at 8 days postinfection.

Abbreviation: ND, not determined.

*

Without any in vitro stimulation, antiviral CTL activity exhibited by spleen, PBMCs, and bone marrow cells was determined by measuring specific 51Cr release from either uninfected or LCMV-infected targets at the indicated effector:target (E:T) ratios.

Lytic units (LU) ar defined as the number of effector cells required to exhibit 20% lysis of infected targets. The spleen and PBMCs contained approximately 30% CD8+ T cells, and CD8+ T cells accounted for about 2.0% of total cells in the bone marrow. LU per total organ were calculated based on total cells recovered from spleen, were estimated for bone marrow from 2 femurs (∼12% of total bone marrow27 ), and were estimated for PBMCs assuming 2.5 mL circulating blood per adult mouse.

Data pooled from 3 mice.

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