Need for an External Proficiency Testing Program for Cytokines, Chemokines, and Plasma Markers of Immune Activation

Author:

Fahey John L.1,Aziz Najib1,Spritzler John2,Plaeger Susan1,Nishanian Parunag1,Lathey Janet L.3,Seigel Joan4,Landay Alan L.4,Kilarui Rakhi5,Schmitz John L.5,White Carmen6,Wara Diane W.6,Akridge Robert7,Cutili Joie8,Douglas Steven D.8,Reuben James9,Shearer William T.9,Nokta Mustafa10,Polland Richard10,Schooley Robert11,Asthana Deshratn12,Mizrachi Yaffa13,Waxdal Myron14

Affiliation:

1. University of California, Los Angeles,1

2. Statistical and Data Analysis Center, Harvard School of Public Health, Boston, Massachusetts2;

3. University of California, San Diego,3 and

4. Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois4;

5. University of North Carolina, Chapel Hill, North Carolina5;

6. University of California, San Francisco,6

7. University of Washington, Seattle, Washington7;

8. Children's Hospital of Philadelphia, Philadelphia Pennsylvania8;

9. MD Anderson Cancer Center and Baylor College of Medicine, Houston,9 and

10. University of Texas Medical Branch, Galveston,10 Texas;

11. University of Colorado Health Sciences Center, Denver, Colorado11;

12. University of Miami School of Medicine, Miami, Florida12;

13. Albert Einstein Medical Center New York, New York13; and

14. FAST Systems, Gaithersburg, Maryland14

Abstract

ABSTRACT An external evaluation program for measuring the performance of laboratories testing for cytokines and immune activation markers in biological fluids was developed. Cytokines, chemokines, soluble cytokine receptors, and other soluble markers of immune activation (CSM) were measured in plasma from a healthy human immunodeficiency virus (HIV)-seronegative reference population and from HIV-seropositive individuals as well as in supernatant fluids from in vitro-stimulated human immune cells. The 14 components measured were tumor necrosis factor (TNF) alpha, gamma interferon, interleukin-1 (IL-1), IL-2, IL-4, IL-6, IL-10, Rantes, MIP-Ia, MIP-Iβ, soluble TNF receptor II, soluble IL-2 receptor alpha, β 2 -microglobulin, and neopterin. Twelve laboratories associated with the Adult and Pediatric AIDS Clinical Trial Groups participated in the study. The performance features that were evaluated included intralaboratory variability, interlaboratory variability, comparison of reagent sources, and ability to detect CSM in the plasma of normal subjects as well as the changes occurring in disease. The principal findings were as follows: (i) on initial testing, i.e., before participating in the program, laboratories frequently differed markedly in their analytic results; (ii) the quality of testing of a CSM in individual participating laboratories could be assessed; (iii) most commercial kits allowed distinction between normal and abnormal plasma CSM levels and between supernatants of stimulated and unstimulated cells; (iv) different sources of reagents and reference standards frequently provided different absolute values; (v) inexperienced laboratories can benefit from participating in the program; (vi) laboratory performance improved during active participation in the program; and (vii) comparability between analyses conducted at different sites can be ensured by an external proficiency testing program.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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