Standardization and performance evaluation of mononuclear cell cytokine secretion assays in a multicenter study
Open Access
- 12 December 2006
- journal article
- research article
- Published by Springer Nature in BMC Immunology
- Vol. 7 (1) , 29-12
- https://doi.org/10.1186/1471-2172-7-29
Abstract
Background: Cryopreservation of peripheral blood mononuclear cells has been used to preserve and standardize immunologic measurements for multicenter studies, however, effects of cryopreservation on cytokine responses are incompletely understood. In designing immunologic studies for a new multicenter birth cohort study of childhood asthma, we performed a series of experiments to determine the effects of two different methods of cryopreservation on the cytokine responses of cord and peripheral blood mononuclear cells. Results: Paired samples of PBMC were processed freshly, or after cryopreservation in a Nalgene container (NC) or a controlled-rate freezer (CRF). Although there were some differences between the methods, cryopreservation inhibited PHA-induced IL-10 secretion and Der f 1-induced IL-2 secretion, and augmented PHA-induced IL-2 secretion and spontaneous secretion of TNF-α. In separate experiments, NC cryopreservation inhibited secretion of several cytokines (IL-13, IL-10, IFN-γ, TNF-α) by PHA-stimulated cord blood mononuclear cells. With the exception of PHA-induced IL-13, results from fresh and cryopreserved cord blood samples were not significantly correlated. Finally, in reproducibility studies involving processing of identical cell samples in up to 4 separate laboratories, variances in cytokine responses of fresh cells stimulated at separate sites did not exceed those in cryopreserved cells stimulated at a central site. Conclusion: Collectively, these studies indicate that cryopreservation can affect mononuclear cell cytokine response profiles, and that IL-10 secretion and antigen-induced responses may be especially vulnerable. These studies also demonstrate that mononuclear cell responses can be standardized for performance in a small number of laboratories for multicenter studies, and underscore the importance of measuring reproducibility and of testing whether cryopreservation techniques alter specific immunologic outcomes.Keywords
This publication has 16 references indexed in Scilit:
- Maximizing the retention of antigen specific lymphocyte function after cryopreservationJournal of Immunological Methods, 2005
- Impact of cryopreservation on tetramer, cytokine flow cytometry, and ELISPOTBMC Immunology, 2005
- Results of an ELISPOT Proficiency Panel Conducted in 11 Laboratories Participating in International Human Immunodeficiency Virus Type 1 Vaccine TrialsAIDS Research and Human Retroviruses, 2005
- CD4+ and CD8+ cells in cryopreserved human PBMC maintain full functionality in cytokine ELISPOT assaysJournal of Immunological Methods, 2003
- Effects of cryopreservation on lymphocyte immunophenotype and functionJournal of Immunological Methods, 2003
- Enhanced ELISPOT detection of antigen-specific T cell responses from cryopreserved specimens with addition of both IL-7 and IL-15—the Amplispot assayJournal of Immunological Methods, 2002
- Use of overlapping peptide mixtures as antigens for cytokine flow cytometryJournal of Immunological Methods, 2001
- Preservation of Lymphocyte Immunophenotype and Proliferative Responses in Cryopreserved Peripheral Blood Mononuclear Cells from Human Immunodeficiency Virus Type 1-Infected Donors: Implications for Multicenter Clinical TrialsClinical and Diagnostic Laboratory Immunology, 2000
- Use of cryopreserved lymphocytes for assessment of the immunological effects of interferon therapy in renal cell carcinoma patientsJournal of Immunological Methods, 1997
- Cryopreservation of human lymphocyte function as measured byin vitro assaysInternational Journal of Cancer, 1976