Inhibition of Leukocyte Migration by a Human Colon Cancer Extract

1981 ◽  
Vol 67 (3) ◽  
pp. 163-167 ◽  
Author(s):  
Maria Caterina Sirianni ◽  
Giuseppe Luzi ◽  
Claudio Iavarone ◽  
Marisa Papaluca ◽  
Massimo Fiorilli ◽  
...  

The direct leucocyte migration inhibition test in capillary tubes was used to test 10 patients with colonic adenocarcinoma against KCl soluble extracts of an allogenic colon cancer and an allogenic normal colon fragment. Inhibition was consistently found with the cancer extract but not with the normal tissue extract. None of the control group of patients affected by other tumors, intestinal and liver disorders showed a migration inhibition in response to the colonic tumor extract. Our findings strongly suggest the presence of a tumor-associated antigen in the cancer extract.

1984 ◽  
Vol 42 (2) ◽  
pp. 132-139 ◽  
Author(s):  
Terezinha C. B. Montelli ◽  
Norma G. S. Mota ◽  
M. Terezinha S. Peraçoli ◽  
Elza A. Torres ◽  
M. Thereza Rezkallah-Iwasso

Cell-mediated and humoral immunity were investigated in 18 patients with West syndrome, 12 with Lennox-Gastaut syndrome and 19 healthy controls. The study included determination of Ô and  peripheral blood lymphocytes, serum levels of IgG, IgA and IgM, skin sensibilization with DNCB, intracutaneous PHA, leucocyte migration inhibition test and lymphocyte blastic transformation in the presence of PHA. Cell-mediated deficiency was detected in 28 children whereas low levels of immunoglobulins were observed only in 6 children. Immunological disturbances were more prominent in children with West syndrome.


1978 ◽  
Vol 54 (8) ◽  
pp. 909-920
Author(s):  
Susumu SAKAGUCHI ◽  
Michio NAKAZAWA ◽  
Syuji NAKAMURA ◽  
Yasuko KONO ◽  
Hideo HAZEKI ◽  
...  

2014 ◽  
Vol 32 (3_suppl) ◽  
pp. 518-518
Author(s):  
Luo Cong

518 Background: Anti-angiogenic therapy is an important therapeutic strategy in advanced colorectal cancer. However, the anti-angiogenic drug,such as bevacizumab(avastin) is expensive. So, clarifying whether different doses of avastin play the same effect in vivo is urgently needed. The aim of the study was to observe the different doses of avastin in combination with irinotecan in human colon tumor growth in nude mice and tumor angiogenesis. Methods: 21 nude mice inoculated with DLD-1 human colon cancer cells were randomly divided into four groups: sterile saline control (group A), 5mg/kg avastin plus irinotecan chemotherapy group (group B), 10mg/kg avastin plus irinotecan group (group C), and irinotecan chemotherapy group (group D). Drugs were administered in the first 1,5,9 days, mice were sacrificed in the 10th day after treatment, the tumor growth inhibitory rate was calculated and the tumor microvessel density (MVD) were detected by immunohistochemistry. Results: The tumor inhibition rate in groups B, C, and D were 62.85%, 47.91%, 39.59% respectively. A, B, C, and D groups’ MVD were 7.000 ± 0.71, 4.940 ± 0.58, 5.080 ± 1.25, 5.557 ± 2.04, The MVD in group B and C were significant different compared with group A by Dunnett's test, and the MVD expression difference between D, A groups and B, C groups did not reach statistical significance (P values were 0.086,0.083). Tissue necrosis was found in each group after HE staining of tumor tissue. Among them, the control group, mostly mild to moderate necrosis, and the necrosis area were increased after drug treatment. But there were no statistical differences of the necrotic area in drug treated groups graded by rank sum test (χ2 = 4.73, P = 0.193). And cell apoptosis was obviously seen in treated groups. Conclusions: Different doses of avastin with irinotecan inhibited the tumor growth on DLD-1 xenografted nude mice, Synergistic effects were observed in combination therapy, From cell morphology changes after staining with HE, we speculated that the mechanism may be related to the inhibition of tumor angiogenesis, and cell apoptosis increasing. The effect of 5mg/kg and 10mg/kg bevacizumab on tumor volume and MVD had no significant differences.


Gut ◽  
1983 ◽  
Vol 24 (4) ◽  
pp. 311-317 ◽  
Author(s):  
F G Simpson ◽  
H P Field ◽  
P D Howdle ◽  
D A Robertson ◽  
M S Losowsky

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