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Clinical Services Program

Contact for Information and Services:

Dr. Michael W. Baseler, Manager
SAIC Frederick, Inc.
301-846-5217                FAX: 301-846-5224
E-mail:
mbaseler@ncifcrf.gov

Mission:

The primary mission of the CSP is to perform sequential studies of immune function in patients with cancer, AIDS, chronic granulomatous disease (CGD) or chronic fatigue syndrome (CFS) during treatment with biological response modifiers or other potential anticancer or antiviral agents. Alterations in immune function are correlated with the patient's clinical response to treatment, and are used to design second-generation clinical studies and guide basic research into the agent's mechanisms of action.

Expertise: The Clinical Services Program (CSP) was established in late 1981 to provide dedicated laboratory facilities to the Biological Response Modifiers Program, National Cancer Institute. During the next decade, the CSP was expanded to provide a full range of dedicated laboratory and clinical facilities to the Medicine Branch, HIV Adult Malignancy Branch, and Surgery Branch, Division of Clinical Sciences, the Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, the Biological Resources Branch, Division of Cancer Treatment and Diagnosis, the Laboratories of Immunoregulation, Clinical Investigations and Host Defenses and the Division of Intramural Research, National Institute of Allergy and Infectious Disease.

The organization of the CSP has evolved and expanded over the last 19 years, so that each laboratory/administrative component is structured to adapt to specific technical work scope requirements in support of the various government programs. A highly trained scientific staff, a centralized administrative and computer programming support staff, and state-of-the art laboratories and clinical facilities allow for comprehensive immunological monitoring and research programs in support of diverse clinical trials. The CSP comprises 13 individual laboratories and a centralized administrative group, with each laboratory responsible for defined areas of the workscope. Technical staff have been cross-trained in a wide variety of immunological procedures, and equipment resources are shared, where appropriate, resulting in the most efficient use of labor and resources. The CSP has gained a reputation as a benchmark laboratory for this type of work.

Established Technologies:

  • Two, three, and four-color flow cytometric phenotypic analysis of peripheral blood, mononuclear cells and cell lines.

  • Two and three-color cell sorting using flow cytometry.
  • Lymphokine and cytokine testing.
  • Blast transformation assays.
  • Cytotoxic assays.
  • Viral burden assays (quantitative PCR, bDNA, NASBA, p24 antigen and RT PCR).
  • Quantitation of stem cells from peripheral blood and bone marrow samples.
  • Production of activated NK and T cells ex vivo for reinfusion into patients.
  • Complete assessments of granulocyte and monocyte function.

New Technologies Under Development:

  • ELISPOT
  • DNA Microarray technologies

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