Characterization of Infused CTLs
Subject . | Class I HLA . | Dominant CTL Epitopes* . | HIV-Specific % Cytotoxicity of Infused Cells† . | ||||
---|---|---|---|---|---|---|---|
. | A . | B . | . | Anti-gp 160 . | Anti-gag . | Anti-RT . | Anti-nef . |
202 | ND | gp 120 aa209-228: TQACPKVSFEPIPIHYCAPA | 40 | 5 | 3 | 53 | |
nef aa61-80: EEEEVGFVTPQVPLRPMTY | |||||||
nef aa101-120: TSLLHPVSLHGMDDPEREVL | |||||||
204 | 2,3 | 8,62 | gp120 aa49-68:VPVWKEATTTLFCASDAKAY | 44 | 33 | 7 | ND |
p24 aa253-272: NPPIPGEIKRWIILGNIK | |||||||
p24 aa293-312: FRDYVDRFYKTLRAEQASQD | |||||||
nef aa101-120: HSQRRQDILDLWIYHTQGYF | |||||||
216 | 2,3 | 14,44 | p24 aa 173-192: SALSEGATPQDLNTMLNTVG | 10 | 30 | 6 | ND |
203 | 3,24 | 8,55 | p17 aa91-105: CRIDVKDTKEALEKIE | 13 | 37 | 7 | ND |
p24 aa323-342: VQNANPDCKTILKALGPAAT | |||||||
214 | 2,−‡ | 21,−‡ | gp120 aa59-78: LFCASDAKAYDTEVHNVWAT | 25 | 48 | 1 | 29 |
gp120 aa69-88: DTEVHNVWATHACVPTDPN | |||||||
gp120 aa119-139: WDQSLKPCVKLTPLCVSLK | |||||||
gp 120 aa199-219: SLTSCNTSVITQACPKVSFE | |||||||
gp120 aa249-268: VSTVQCTHGIRPVVSTQLLL | |||||||
p24 aa153-172: NAWVKVVEEKAFSPEVIPMF | |||||||
p24 aa163-182: AFSPEVIPMFSALSEGATPQ | |||||||
p24 aa203-222: ETINEEAAEQDRVHPVVHAGP | |||||||
nef aa101-120: HSQRRQDILDLWIYHTQGYF | |||||||
nef aa111-132: LWIYHTQGYFPDWQNYTPGPGV | |||||||
nef aa121-140: PDWQNYTPGPGVRYPLTFGW | |||||||
nef aa121-140: GMDDPEREVLEWRFDSRLAF | |||||||
226 | 11,24 | 8,53 | nef aa61-80: EEEEVGFPVTPQVPLRPMTY | 3 | 7 | 4 | 28 |
nef aa71-90: PQVPLRPMTYKAAVDLSHFL | |||||||
nef aa81-100: KAAVDLSHLKEKGGLEGLI |
Subject . | Class I HLA . | Dominant CTL Epitopes* . | HIV-Specific % Cytotoxicity of Infused Cells† . | ||||
---|---|---|---|---|---|---|---|
. | A . | B . | . | Anti-gp 160 . | Anti-gag . | Anti-RT . | Anti-nef . |
202 | ND | gp 120 aa209-228: TQACPKVSFEPIPIHYCAPA | 40 | 5 | 3 | 53 | |
nef aa61-80: EEEEVGFVTPQVPLRPMTY | |||||||
nef aa101-120: TSLLHPVSLHGMDDPEREVL | |||||||
204 | 2,3 | 8,62 | gp120 aa49-68:VPVWKEATTTLFCASDAKAY | 44 | 33 | 7 | ND |
p24 aa253-272: NPPIPGEIKRWIILGNIK | |||||||
p24 aa293-312: FRDYVDRFYKTLRAEQASQD | |||||||
nef aa101-120: HSQRRQDILDLWIYHTQGYF | |||||||
216 | 2,3 | 14,44 | p24 aa 173-192: SALSEGATPQDLNTMLNTVG | 10 | 30 | 6 | ND |
203 | 3,24 | 8,55 | p17 aa91-105: CRIDVKDTKEALEKIE | 13 | 37 | 7 | ND |
p24 aa323-342: VQNANPDCKTILKALGPAAT | |||||||
214 | 2,−‡ | 21,−‡ | gp120 aa59-78: LFCASDAKAYDTEVHNVWAT | 25 | 48 | 1 | 29 |
gp120 aa69-88: DTEVHNVWATHACVPTDPN | |||||||
gp120 aa119-139: WDQSLKPCVKLTPLCVSLK | |||||||
gp 120 aa199-219: SLTSCNTSVITQACPKVSFE | |||||||
gp120 aa249-268: VSTVQCTHGIRPVVSTQLLL | |||||||
p24 aa153-172: NAWVKVVEEKAFSPEVIPMF | |||||||
p24 aa163-182: AFSPEVIPMFSALSEGATPQ | |||||||
p24 aa203-222: ETINEEAAEQDRVHPVVHAGP | |||||||
nef aa101-120: HSQRRQDILDLWIYHTQGYF | |||||||
nef aa111-132: LWIYHTQGYFPDWQNYTPGPGV | |||||||
nef aa121-140: PDWQNYTPGPGVRYPLTFGW | |||||||
nef aa121-140: GMDDPEREVLEWRFDSRLAF | |||||||
226 | 11,24 | 8,53 | nef aa61-80: EEEEVGFPVTPQVPLRPMTY | 3 | 7 | 4 | 28 |
nef aa71-90: PQVPLRPMTYKAAVDLSHFL | |||||||
nef aa81-100: KAAVDLSHLKEKGGLEGLI |
Dominant CTL epitopes were identified using mitogen-stimulated T-cell lines derived from PBMCs at the time of enrollment (see the Materials and Methods). Up to three dominant epitope peptides were used to selectively expand T cells for infusion.
Abbreviation: ND, not done.
Epitopes used to expand the infused cells are in bold. Epitopes recognized by CTLs are likely to be 8- to 11-aa peptides contained in the larger peptides used for screening. These epitopes, based on the sequences of laboratory isolates of HIV, are in relatively conserved regions of the virus. Patients may also recognize additional epitopes in variable regions of the isolates with which they are infected. Epitopes defined for two overlapping peptides may be contained in the 10-aa overlap region. Amino acid numbering as in Ratner et al.40
Data are for 4-hour CTL assay performed at an E:T ratio of 10:1. Targets were either preincubated with HIV peptides (for nef peptides only) or infected with HIV-vaccinia recombinants (see the Materials and Methods). Background lysis of targets preincubated with no peptide or infected with vaccinia-lacZ, respectively, was subtracted for HIV-specific percent cytotoxicity.
Unambiguous tissue typing for the second allele of this patient was not possible.