CTL activity against antigens derived from KSHV and EBV
Antigen . | Cohort . | ||
---|---|---|---|
MM . | KSHV-positive* . | KSHV-negative . | |
KSHV ORF73 | 0/16 | 10/141-153 | 0/10 |
KSHV ORF65 | 0/16 | 8/14 | 0/10 |
MM ORF65† | 0/16 | 2/14 | 0/10 |
EBV‡ | 16/16 | 14/14 | 10/10 |
Antigen . | Cohort . | ||
---|---|---|---|
MM . | KSHV-positive* . | KSHV-negative . | |
KSHV ORF73 | 0/16 | 10/141-153 | 0/10 |
KSHV ORF65 | 0/16 | 8/14 | 0/10 |
MM ORF65† | 0/16 | 2/14 | 0/10 |
EBV‡ | 16/16 | 14/14 | 10/10 |
Values are numbers of patients.
KSHV positivity was determined by latency-associated nuclear antigen-specific serologic assessment as described previously.2
The MM ORF65 antigen pool included the 4 peptides spanning the described MM-KSHV ORF65 sequence C-terminal to the stop codon in the previously reported ORF65.
Only those with a response to EBV are included in the table. However, 11 patients with MM who had no response to EBV were also negative for ORF65-specific and ORF73-specific responses on ELISPOT assays.
ELISPOT responses were considered positive if values were higher than 15 spot-forming cells (SFCs)/106 PBMCs. The range for positive ORF73-specific responses was 257 to 1280 SFCs/106 PBMCs, that for ORF65-specific responses was 40 to 120 SFCs/106 PBMCs, and that for positive EBV responses was 25 to 1500 SFCs/106 PBMCs.