Naturally occurring and therapy-induced antibodies to human granulocyte colony-stimulating factor (G-CSF) in human serum

Sera were obtained from two groups of patients. Group A included 7 patients with low‐grade non‐Hodgkin's lymphoma treated with three or more cycles of standard‐dose chemotherapy and recombinant human granulocyte‐colony stimulating factor (rhG‐CSF). The cytokine was administered to half the pati...

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Published inJournal of cellular physiology Vol. 173; no. 2; pp. 219 - 226
Main Authors Laricchia-Robbio, Leopoldo, Moscato, Stefania, Genua, Angelo, Liberati, Anna Marina, Revoltella, Roberto P.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.11.1997
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Summary:Sera were obtained from two groups of patients. Group A included 7 patients with low‐grade non‐Hodgkin's lymphoma treated with three or more cycles of standard‐dose chemotherapy and recombinant human granulocyte‐colony stimulating factor (rhG‐CSF). The cytokine was administered to half the patients after the first chemotherapy cycle and to the other half after the second according to a randomized design and then to all patients from the third chemotherapy cycle on, until documented hemopoietic reconstitution. Group B included 3 patients with high‐grade non‐Hodgkin's lymphoma, 1 patient with resistant Hodgkin's disease, and 1 patient with multiple myeloma who received high‐dose chemotherapy and rhG‐CSF. Anti‐G‐CSF antibodies were detected in the sera of 4 patients. Both immunoglobulin IgM and IgG antibodies were detected at low levels in pretreatment sera from one group A patient. IgG antibody titers increased markedly during the first and second periods of G‐CSF administration. IgG class antibodies developed in 3 group B patients during the first course of rhG‐CSF administration. Circulating anti‐G‐CSF antibodies did not seem to affect hematological recovery. Low levels of anti‐G‐CSF antibodies were also detected in sera (15/135) from different healthy adults and in sera (5/40) from umbilical cord blood. Saturable antibody binding and competition enzyme‐linked immunosorbent assay (ELISA) and immunoblotting confirmed antibody specificity. J. Cell. Physiol. 173:219–226, 1997. © 1997 Wiley‐Liss, Inc.
Bibliography:European Science Foundation: "Artificial Biosensing Interfaces" Programme
European Union - No. EV 5-CT 94-0407
CNR-PB "Italy-Sweden"
ArticleID:JCP25
ark:/67375/WNG-2F3FRFM0-9
istex:CDB45AEA2D90AB36358F39EC8FE65DF2E2C08AD0
ISSN:0021-9541
1097-4652
DOI:10.1002/(SICI)1097-4652(199711)173:2<219::AID-JCP25>3.0.CO;2-9