CONSTITUTIVE RELEASE OF IL6 BY HUMAN PAPILLOMAVIRUS TYPE-16 (HPV16)-HARBORING KERATINOCYTES - A MECHANISM AUGMENTING THE NK-CELL-MEDIATED LYSIS OF HPV-BEARING NEOPLASTIC-CELLS

被引:39
作者
MALEJCZYK, J
MALEJCZYK, M
URBANSKI, A
KOCK, A
JABLONSKA, S
ORTH, G
LUGER, TA
机构
[1] WARSAW ACAD MED & HOSP, DEPT DERMATOL, PL-02008 WARSAW, POLAND
[2] INST PASTEUR, INSERM, INSERM, U190, UNITE PAPILLOMAVIRUS, F-75724 PARIS 15, FRANCE
[3] UNIV VIENNA, DEPT DERMATOL 2,CELL BIOL LAB, LUDWIG BOLTZMANN INST,DVS, A-1090 VIENNA, AUSTRIA
[4] UNIV MUNSTER, DEPT DERMATOL, W-4400 MUNSTER, GERMANY
关键词
D O I
10.1016/0008-8749(91)90390-W
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the present study we demonstrate that the cultured human keratinocyte cell line (SK-v cells) harboring and expressing integrated human papillomavirus type 16 (HPV16) DNA sequences constitutively releases IL6, which is known as a pleiotropic immunoregulatory cytokine of potential antitumor properties. The presence of IL6 activity in SK-v cell-conditioned media (SK-v CM) was demonstrated by tritiated thymidine incorporation into IL6-dependent B9 murine plasma-cytoma cells. The effect on B9 cells was specific since it could be inhibited by anti-IL6 neutralizing antibodies but not by a normal control serum. IL6 did not affect SK-v cell growth; however, it significantly augmented NK cell activity of human peripheral blood lymphocytes against both K562 erytholeukemic and SK-v cells as assessed by 51Cr release assay. SK-v CM displayed NK cell-augmenting activity that copurified with IL6 activity in both size exclusion and anion-exchange HPLC. Furthermore, SK-v cell-derived NK cell stimulatory activity could be neutralized with anti-IL6 antibodies. These results suggest that HPV-harboring neoplastic cells can release IL6 which may indirectly mediate tumor death by augmentation of NK cell activity. © 1991.
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页码:155 / 164
页数:10
相关论文
共 46 条
[21]   NATURAL ANTI-CHONDROCYTE CYTO-TOXICITY OF NORMAL HUMAN PERIPHERAL-BLOOD MONONUCLEAR-CELLS [J].
MALEJCZYK, J .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1989, 50 (01) :42-52
[22]   ABROGATED NK-CELL LYSIS OF HUMAN PAPILLOMAVIRUS (HPV)-16-BEARING KERATINOCYTES IN PATIENTS WITH PRE-CANCEROUS AND CANCEROUS HPV-INDUCED ANOGENITAL LESIONS [J].
MALEJCZYK, J ;
MAJEWSKI, S ;
JABLONSKA, S ;
ROGOZINSKI, TT ;
ORTH, G .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (02) :209-214
[23]  
MALEJCZYK J, UNPUB
[24]  
MAY LT, 1988, J BIOL CHEM, V263, P7760
[25]   INTERLEUKIN-6 (IL-6) FUNCTIONS AS AN INVITRO AUTOCRINE GROWTH-FACTOR IN RENAL-CELL CARCINOMAS [J].
MIKI, S ;
IWANO, M ;
MIKI, Y ;
YAMAMOTO, M ;
TANG, B ;
YOKOKAWA, K ;
SONODA, T ;
HIRANO, T ;
KISHIMOTO, T .
FEBS LETTERS, 1989, 250 (02) :607-610
[26]   AIDS KAPOSI SARCOMA-DERIVED CELLS PRODUCE AND RESPOND TO INTERLEUKIN-6 [J].
MILES, SA ;
REZAI, AR ;
SALAZARGONZALEZ, JF ;
VANDERMEYDEN, M ;
STEVENS, RH ;
LOGAN, DM ;
MITSUYASU, RT ;
TAGA, T ;
HIRANO, T ;
KISHIMOTO, T ;
MARTINEZMAZA, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4068-4072
[27]   ANTITUMOR-ACTIVITY OF RECOMBINANT INTERLEUKIN-6 IN MICE [J].
MULE, JJ ;
MCINTOSH, JK ;
JABLONS, DM ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (03) :629-636
[28]   THE ESSENTIAL ROLE OF B-CELL STIMULATORY FACTOR-II (BSF-2/IL-6) FOR THE TERMINAL DIFFERENTIATION OF B-CELLS [J].
MURAGUCHI, A ;
HIRANO, T ;
TANG, B ;
MATSUDA, T ;
HORII, Y ;
NAKAJIMA, K ;
KISHIMOTO, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (02) :332-344
[29]  
NAKAJIMA K, 1989, J IMMUNOL, V142, P531
[30]   BOWENOID PAPULOSIS OF THE MALE AND FEMALE GENITALIA - RISK OF CERVICAL NEOPLASIA [J].
OBALEK, S ;
JABLONSKA, S ;
BEAUDENON, S ;
WALCZAK, L ;
ORTH, G .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1986, 14 (03) :433-444