TY - JOUR
T1 - Nucleotide sequence analysis of a human monoclonal antibody 22-13 reactive with lung tumor-associated antigen
AU - Numasaki, Muneo
AU - Nakamura, Kazuyasu
AU - Fukuoka, Yoshihiro
AU - Sato, Nobuyuki
AU - Saeki, Hisaaki
AU - Tachibana, Takehiko
AU - Hanai, Nobuo
AU - Nukiwa, Toshihiro
AU - Kudo, Toshio
PY - 1998/2
Y1 - 1998/2
N2 - A human monoclonal antibody (HuMAb) 22-13 (IgG1, κ) recognizes a cytoplasmic antigen associated primarily with human lung tumors. This study reports the primary nucleotide and deduced amino acid sequences of the rearranged heavy and light chains of the HuMAb 22-13. This HuMAb uses a V(H) gene member of the V(H)Ia gene family, 51P1 and is productively rearranged with a D-D fusion product of the D(LR)2 and D(XP)2 germ line D(H) genes and the germ line J(H)3 gene. HuMAb 22-13 V(κ) belongs to the κ light chain variable subgroup IIIb family and appears to be derived from the Humkv325 germ line gene and is rearranged with a germ line J(κ)5 gene. The results reveal that production of a HuMAb 22-13 is achieved by rearrangement of the 51P1/Humkv325 germ line variable region gene combination, associated with the autoimmune repertoire and that HuMAb 22-13 has a striking sequence homology to rheumatoid factors (RFs) of the Wa idiotypic family. HuMAb 22-13 and Wa RFs have in common V(H)Ia and V(κ)IIIb gene segments, but use different D(H), J(H) and J(κ) gene segments. However, in spite of this structural similarity, HuMAb 22-13 does not display rheumatoid factor activity. Taken together with the reported findings, these data indicate the representation of the shared usage of highly homologous variable region genes in entirely different humoral immune responses in the human system.
AB - A human monoclonal antibody (HuMAb) 22-13 (IgG1, κ) recognizes a cytoplasmic antigen associated primarily with human lung tumors. This study reports the primary nucleotide and deduced amino acid sequences of the rearranged heavy and light chains of the HuMAb 22-13. This HuMAb uses a V(H) gene member of the V(H)Ia gene family, 51P1 and is productively rearranged with a D-D fusion product of the D(LR)2 and D(XP)2 germ line D(H) genes and the germ line J(H)3 gene. HuMAb 22-13 V(κ) belongs to the κ light chain variable subgroup IIIb family and appears to be derived from the Humkv325 germ line gene and is rearranged with a germ line J(κ)5 gene. The results reveal that production of a HuMAb 22-13 is achieved by rearrangement of the 51P1/Humkv325 germ line variable region gene combination, associated with the autoimmune repertoire and that HuMAb 22-13 has a striking sequence homology to rheumatoid factors (RFs) of the Wa idiotypic family. HuMAb 22-13 and Wa RFs have in common V(H)Ia and V(κ)IIIb gene segments, but use different D(H), J(H) and J(κ) gene segments. However, in spite of this structural similarity, HuMAb 22-13 does not display rheumatoid factor activity. Taken together with the reported findings, these data indicate the representation of the shared usage of highly homologous variable region genes in entirely different humoral immune responses in the human system.
KW - Autoimmune repertoire
KW - Human monoclonal antibody
KW - Rheumatoid factor
KW - Tumor-associated antigen
KW - Variable region gene
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U2 - 10.1016/S0165-2478(97)00141-7
DO - 10.1016/S0165-2478(97)00141-7
M3 - Article
C2 - 9557952
AN - SCOPUS:0032007803
SN - 0165-2478
VL - 60
SP - 111
EP - 120
JO - Immunology Letters
JF - Immunology Letters
IS - 2-3
ER -