TY - JOUR
T1 - Clinical relevance of the venom-specific immunoglobulin G antibody level during immunotherapy
AU - Golden, David B.K.
AU - Meyers, Deborah A.
AU - Kagey-Sobotka, Anne
AU - Valentine, Martin D.
AU - Lichtenstein, Lawrence M.
N1 - Funding Information:
From the Division of Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, The Good Samaritan Hospital, Baltimore, Md. Supported by NIH grant AI 08270 and by a fellowship grant from the Medical Research Council of Canada. Publication No. 468 from the O’Neill Laboratories, tan Hospital, Baltimore, Md. Received for publication Oct. 20, 198 1. Accepted for publication March 1, 1982. Reprint requests to: David B. K. Golden, M.D., Johns Hopkins University School of Medicine, The Good Samaritan Hospital, 5601 Loch Raven Blvd., Baltimore, MD 21239.
PY - 1982/6
Y1 - 1982/6
N2 - Parameters associated with successful venom immunotherapy in insect allergy were sought by comparison of treatment failures with successes. Half-dose treatment was completely protective in 32 patients (successes) but was only partially effective in eight (failures). The outcome of treatment was not related to the severity of pretreatment sting reactions, to the degree of skin-test sensitivity, to an atopic personal history, or to age or gender. The mean yellow jacket venom-specific IgG antibody level (by the Staph-A solid-phase radioimmunoassay) was significantly less in the failures (3.9 ± 0.6 μg/ml) than in the successes (7.3 ± 1.1 μg/ml) (p < 0.01). When the failures were successfully treated, their mean IgG level (6.1 ± 1.3 μg/ml) was significantly greater than that associated with treatment failure (p < 0.025). Patients with an IgG antibody level above 5.0 μg/ml were significantly more likely to be fully protected (p < 0.02). Those whose IgG levels were less than 5 μg/ml had a risk of reaction similar to that in untreated patients. We conclude that early in the maintenance phase of low-dose venom immunotherapy, the risk of a reaction to a challenge sting is significantly greater for those patients with low levels of venom-specific IgG antibodies.
AB - Parameters associated with successful venom immunotherapy in insect allergy were sought by comparison of treatment failures with successes. Half-dose treatment was completely protective in 32 patients (successes) but was only partially effective in eight (failures). The outcome of treatment was not related to the severity of pretreatment sting reactions, to the degree of skin-test sensitivity, to an atopic personal history, or to age or gender. The mean yellow jacket venom-specific IgG antibody level (by the Staph-A solid-phase radioimmunoassay) was significantly less in the failures (3.9 ± 0.6 μg/ml) than in the successes (7.3 ± 1.1 μg/ml) (p < 0.01). When the failures were successfully treated, their mean IgG level (6.1 ± 1.3 μg/ml) was significantly greater than that associated with treatment failure (p < 0.025). Patients with an IgG antibody level above 5.0 μg/ml were significantly more likely to be fully protected (p < 0.02). Those whose IgG levels were less than 5 μg/ml had a risk of reaction similar to that in untreated patients. We conclude that early in the maintenance phase of low-dose venom immunotherapy, the risk of a reaction to a challenge sting is significantly greater for those patients with low levels of venom-specific IgG antibodies.
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U2 - 10.1016/0091-6749(82)90172-5
DO - 10.1016/0091-6749(82)90172-5
M3 - Article
C2 - 7076990
AN - SCOPUS:0019976840
SN - 0091-6749
VL - 69
SP - 489
EP - 493
JO - The Journal of Allergy and Clinical Immunology
JF - The Journal of Allergy and Clinical Immunology
IS - 6
ER -