TY - JOUR
T1 - Early appearance and activation of natural killer cells in tumor‐infiltrating lymphoid cells during tumor development
AU - Kurosawa, Shin
AU - Matsuzaki, Goro
AU - Harada, Mamoru
AU - Ando, Takashi
AU - Nomoto, Kikuo
PY - 1993/5
Y1 - 1993/5
N2 - We investigated NK cell infiltration into tumor developing lesions at early stage of tumor development after intraperitoneal inoculation of 3LL lung carcinoma into syngeneic C57BL/6 mice. Natural killer (NK) cells, which were detected by anti‐NK 1.1 monoclonal antibody (mAb), remarkably increased in number in tumor‐developing lesions (peritoneal cavity) as early as day 3 after inoculation of 3LL. The tumor‐infiltrating NK cells from 3LL‐inoculated mice produced a high level of interferon‐γ by co‐culture with 3LL and showed enhanced cytotoxic activities against both NK‐sensitive (YAC‐1) and NK‐resistant (3LL and P815) tumors. Furthermore, mice depleted of NK cells by injection of anti‐NK 1.1 mAb or antiasialo GM1 antibody showed shorter survival times after intraperitoneal inoculation of 3LL when compared with control mice. These results suggest that NK cells infiltrate the tumor‐developing lesion at an early stage and may participate in the early protection against tumors through production of a high amount of interferon‐γ and enhanced cytotoxicity at tumor‐bearing sites.
AB - We investigated NK cell infiltration into tumor developing lesions at early stage of tumor development after intraperitoneal inoculation of 3LL lung carcinoma into syngeneic C57BL/6 mice. Natural killer (NK) cells, which were detected by anti‐NK 1.1 monoclonal antibody (mAb), remarkably increased in number in tumor‐developing lesions (peritoneal cavity) as early as day 3 after inoculation of 3LL. The tumor‐infiltrating NK cells from 3LL‐inoculated mice produced a high level of interferon‐γ by co‐culture with 3LL and showed enhanced cytotoxic activities against both NK‐sensitive (YAC‐1) and NK‐resistant (3LL and P815) tumors. Furthermore, mice depleted of NK cells by injection of anti‐NK 1.1 mAb or antiasialo GM1 antibody showed shorter survival times after intraperitoneal inoculation of 3LL when compared with control mice. These results suggest that NK cells infiltrate the tumor‐developing lesion at an early stage and may participate in the early protection against tumors through production of a high amount of interferon‐γ and enhanced cytotoxicity at tumor‐bearing sites.
KW - Natural killer cells
KW - Tumor
KW - Tumor‐infiltrating lymphocytes
UR - http://www.scopus.com/inward/record.url?scp=0027415152&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027415152&partnerID=8YFLogxK
U2 - 10.1002/eji.1830230507
DO - 10.1002/eji.1830230507
M3 - Article
C2 - 8477798
AN - SCOPUS:0027415152
VL - 23
SP - 1029
EP - 1033
JO - European Journal of Immunology
JF - European Journal of Immunology
SN - 0014-2980
IS - 5
ER -