TY - JOUR
T1 - Development of a neutralizing monoclonal antibody against rabbit IL-1 receptor antagonist and utilization for elisa and measurement of masked IL-1 activity in biological materials
AU - Matsukawa, A.
AU - Furukawa, S.
AU - Ohkawara, S.
AU - Takagi, K.
AU - Yoshinaga, M.
N1 - Funding Information:
try of Education, Science and Culture and by a grant from the Ministry of Health and Welfare,
Funding Information:
lent technical assistance. This work was supported in part by a Grant-in-Aid from the Minis-
PY - 1994
Y1 - 1994
N2 - We developed a monoclonal antibody with neutralizing activity against the rabbit IL-1 receptor antagonist (IL-1ra) and a sandwich ELISA for rabbit IL-1ra. Using this ELISA, we measured IL-1ra contents in inflammatory exudate cells and culture supernatants of LPS-stimulated macrophages. The production of IL-1ra occurred rapidly after the onset of inflammation in vivo and after stimulation of macrophages in vitro and was sustained for a long period. The time interval for detection of IL-1 activity overlapped with the above mentioned period of IL-1ra production. In the presence of this neutralizing monoclonal IgG, the effect of IL-1ra in these biological specimens was nil and heretofore unrecognized IL-1 activity in the samples was measurable; the rate of this increment in activity ranging between 1.5- and 4.8-fold. We conclude that underestimations of IL-1 activity have been made and previously reported results on IL-1 activities in many biological materials have to be re-examined.
AB - We developed a monoclonal antibody with neutralizing activity against the rabbit IL-1 receptor antagonist (IL-1ra) and a sandwich ELISA for rabbit IL-1ra. Using this ELISA, we measured IL-1ra contents in inflammatory exudate cells and culture supernatants of LPS-stimulated macrophages. The production of IL-1ra occurred rapidly after the onset of inflammation in vivo and after stimulation of macrophages in vitro and was sustained for a long period. The time interval for detection of IL-1 activity overlapped with the above mentioned period of IL-1ra production. In the presence of this neutralizing monoclonal IgG, the effect of IL-1ra in these biological specimens was nil and heretofore unrecognized IL-1 activity in the samples was measurable; the rate of this increment in activity ranging between 1.5- and 4.8-fold. We conclude that underestimations of IL-1 activity have been made and previously reported results on IL-1 activities in many biological materials have to be re-examined.
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U2 - 10.3109/08820139409087794
DO - 10.3109/08820139409087794
M3 - Article
C2 - 8194853
AN - SCOPUS:0028331801
SN - 0882-0139
VL - 23
SP - 129
EP - 142
JO - Immunological Investigations
JF - Immunological Investigations
IS - 2
ER -