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Effects of radiolabelled murine antibody infusion on TNF‐α, IL‐1β, and soluble IL‐2 receptor in cancer patients
Author(s) -
Gridley Daila S.,
Hammond Samantha N.,
Slater James M.
Publication year - 1994
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.1860080408
Subject(s) - tumor necrosis factor alpha , monoclonal antibody , antibody , medicine , endocrinology , alpha (finance) , interleukin 2 , receptor , cytokine , beta (programming language) , immunology , surgery , construct validity , patient satisfaction , computer science , programming language
This study evaluates the plasma levels of tumor necrosis factor‐α (TNF‐α), interleukin‐ 1β (IL‐1β), and soluble IL‐2 receptor (sIL‐2R) in cancer patients infused with radiolabelled murine monoclonal antibodies (MAbs) for the purposes of imaging and dosimetry. Blood samples were collected from 13 patients (10 with colon cancer and 3 with lung cancer) before and at 4 and 7 days after infusion of either conventional intact 111 In‐ MAb or a bifunctional antibody delivery system. For all subjects, except one, this was the first exposure to murine MAb. Before infusion, higher levels of TNF‐α, IL‐1β, and sIL‐2R than the average expected in the plasma of healthy individuals were found. A significant decrease was noted in TNF‐α when preinfusion concentrations were compared to 4 day ( P < 0.01) or to 7 day ( P < 0.05) postinfusion values. A 50% or greater decrease in IL‐1β was also observed in most individuals with time after infusion. In contrast, sIL‐2R concentrations remained relatively stable during the 1 week follow‐up period. However, strikingly different patterns in the IL‐1β and sIL‐2R levels were noted in the subject who had received two previous murine antibody infusions. Our data show that the administration of radiolabelled murine antibodies, either conventional or bifunctional, can significantly alter plasma levels of TNF‐α and IL‐1β. These cytokines are important in immunoregulation and, perhaps also, in modulation of neoplastic growth. © 1994 Wiley‐Liss, Inc.

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