TABLE 2.
Monoclonal TCR transcriptsa
Patient | Source | V family | V region | CDR3 region | Joining region | J family |
---|---|---|---|---|---|---|
MZ-CC01-1 | CD8+ PBL | VA 9 | SAMYYCA | PASRS | NTGKLIFGQG | AJ 37 |
VA 19 | SAVYICA | VDSR | AAGNKLTFGGG | AJ 17 | ||
VA 22 | SAVYFCA | LSPI | SSGSARQLTFGSG | AJ 22 | ||
CD4+ TIL | VA 2 | SATYLCA | VNTY | SGNTPLVFGKG | AJ 29 | |
VA 5 | SATYLCA | LDQG | DYKLSFGAG | AJ 20 | ||
VA 6 | SAMYFCA | MREGY | SGNTPLVFGKG | AJ 29 | ||
VA 7S2 | SASYLCA | VREQ | AAGNKLTFGGG | AJ 17 | ||
VA 12 | SAVYFCA | PL | TNAGKSTFGDG | AJ 27 | ||
VA 13 | SGVYFCA | V | SGYSTLTFGKG | AJ 11 | ||
VA 21 | SAVYFCA | AKD | QAGTALIFGKG | AJ 15 | ||
VA 24 | SASYICV | VP | NTDKLIFGTG | AJ 34 | ||
VB 5S8 | SALYLCA | SSFRIGY | GYTFGSG | BJ 1-2 | ||
VB 17 | TAFYLCA | SREWGD | TEAFFGQG | BJ 1.1 | ||
MZ-CC01-2 | CD8+ PBL | VA 5 | SATYLCA | LDSR | AAGNKLTFGGG | AJ 17 |
VA 8S2 | SAVYFCA | ENTF | NQGGKLIFGQG | AJ 23 | ||
VA 17 | SATYFCA | ATYV | NSGGGADGLTFGKG | AJ 45 | ||
CD4+ TIL | VA 2 | SATYLCV | VPDGI | NDMRFGAG | AJ 43 | |
VA 13 | SGVYFCA | VERW | ARLMFGDG | AJ 31 | ||
VA 20 | TAVYYCL | VGPLM | NSGGYQKVTFGIG | AJ 13 | ||
VA 22 | SAVYFCA | LKGR | NNNDMRFGAG | AJ 43 | ||
VA 23 | SATYLCA | VR | SGAGSYQLTFGKG | AJ 28 | ||
Tumor | VA 16 | SALYFCA | VRDHS | SGGYNKLIFGAG | AJ 4 | |
VB 7S1 | SALYLCA | SSQEGDL | YEQYFGPG | BJ 2-7 | ||
VB 15 | TALYFCA | TSDSDSGD | TDTQYFGPG | BJ 2-3 | ||
VB 23 | SALYFCA | SSQDN | SYEQYFGPG | BJ 2-7 | ||
MZ-CC01-3 | CD8+ PBL | VA 13 | SGVYFCA | VDAGY | GNEKLTFGTG | AJ 48 |
cDNA was generated from CD4+ and CD8+ PBL, freshly harvested tumor tissue, and CD4+ TIL and tested for monoclonal TCR VA or VB transcripts as described in the text. TCR VA or VB families were characterized for monoclonality by direct sequencing of the amplified product from each TCR family. Note the large number of monoclonal TCR VA mRNA transcripts in CD4+ TIL from patient MZ-CC01-1. Monoclonal TCR transcripts detected in freshly harvested tumor tissue could not be detected in TIL or in PBL. Thus, individual TCR clonotypes could not be expanded in vitro. Short-term (7 days) in vitro culture of T cells (TIL) in the presence of autologous tumor and IL-7 resulted in an oligoclonal T-cell population.