Literature DB >> 1071966

The complement system in tumor immunity: significance of elevated levels of complement in tumor bearing hosts.

K Nishioka, K Kawamura, T Hirayama, T Kawashima, K Shimada.   

Abstract

The elevation of complement level in the sera and depressed state of tuberculin reaction were observed in lung cancer patients. A clinical follow-up study demonstrated negative conversion of tuberculin reaction while keeping the complement at an elevated level during the observation period. This phenomenon can be explained; the complement system is elevated to compensate the depressed cell-mediated system to prevent the immunological surveillance system from invading agents in tumor bearing hosts. The immunological states of the patients with various diseases are classified into six stages according to the tuberculin reactivity, positive or negative, and complement level: elevated, normal, or depressed. A healthy control group is composed of the group of complement normal and tuberculin positive (Stage I). Most of acute inflammation falls into the elevated level of both complement and positive tuberculin reaction (Stage II). Sarcoidosis, leprosy, and Wegener's granulomatosis are divided into the elevated level of complement and depressed tuberculin reaction (Stage III). Systemic lupus erythematosus is in Stage V with the depressed state of both tuberculin reaction and complement level. A follow-up study of lung cancer patients showed a possible chronological sequence starting from Stage I through III, and finally to V, similar to the progression-of-disease process. The biological and medical significance related to the phenomenon is discussed, standing upon immunochemical, phylogenical, and immunogenetical standpoints of complement research.

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Year:  1976        PMID: 1071966     DOI: 10.1111/j.1749-6632.1976.tb41656.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  18 in total

1.  Increases in immunoglobulin and complement in patients with esophageal or gastric cancer.

Authors:  T Saito; A Kuwahara; T Kinoshita; Y Shigemitsu; K Shimoda; M Miyahara; M Kobayashi
Journal:  Surg Today       Date:  1992       Impact factor: 2.549

2.  Effect of malnutrition and nutritional rehabilitation on tuberculin reactivity and complement level in rats.

Authors:  M Sakamoto; K Nishioka; K Shimada
Journal:  Immunology       Date:  1979-10       Impact factor: 7.397

3.  C3 levels in the sera of rabbits infested and reinfested with Ixodes ricinus L. and in midguts of fed ticks.

Authors:  V Papatheodorou; M Brossard
Journal:  Exp Appl Acarol       Date:  1987-03       Impact factor: 2.132

4.  Anaphylatoxin C5a creates a favorable microenvironment for lung cancer progression.

Authors:  Leticia Corrales; Daniel Ajona; Stavros Rafail; Juan J Lasarte; Jose I Riezu-Boj; John D Lambris; Ana Rouzaut; Maria J Pajares; Luis M Montuenga; Ruben Pio
Journal:  J Immunol       Date:  2012-10-01       Impact factor: 5.422

5.  Level of complement activity and components C1, C4, C2, and C3 in complement response to bacterial challenge in malnourished rats.

Authors:  M Sakamoto; S Ishii; K Nishioka; K Shimada
Journal:  Infect Immun       Date:  1981-05       Impact factor: 3.441

Review 6.  The role of the complement system in cancer.

Authors:  Vahid Afshar-Kharghan
Journal:  J Clin Invest       Date:  2017-03-01       Impact factor: 14.808

7.  Complement Synthesis Influencing Factors Produced by Acute Myeloid Leukemia Blast Cells.

Authors:  Béla Schmidt; Márta Válay; Sarolta Nahajevszky; Ervin Pitlik; György Füst
Journal:  Pathol Oncol Res       Date:  1995       Impact factor: 3.201

8.  Cellular immunity and complement levels in hosts with brain tumours.

Authors:  M Matsutani; T Suzuki; T Hori; H Terao; K Takakura; K Nishioka
Journal:  Neurosurg Rev       Date:  1984       Impact factor: 3.042

9.  Total hemolytic complement (CH50) and its fractions (C3 and C4) in the sera of patients with carcinoma of the oral cavity, uterine cervix, and breast.

Authors:  T Vijayakumar; R Ankathil; P Remani; V M Beevi; K K Vijayan; C K Panicker
Journal:  J Clin Immunol       Date:  1987-07       Impact factor: 8.317

10.  Immunological behaviour following rubella infection.

Authors:  Y Niwa; T Kanoh
Journal:  Clin Exp Immunol       Date:  1979-09       Impact factor: 4.330

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