SBIR/STTR Research Award

THE OBJECTIVE OF THE PROPOSED RESEARCH IS TO DEVELOP AN IMMUNOLOGICALLY SPECIFIC ADSORBENT FOR USE IN EXTRACORPOREALSYSTEMS TO REMOVE IMMUNOREACTIVE IGM FROM THE SERUM OF PATIENTS FOR PRIMARY BILIARY CIRRHOSIS (PBC).

Award identifier ee727ce87e3e9890ba4fb942a11f950772339a3e973c66a58901a460846611b4Awarding agency Department of Health and Human Services

Award amount

$26,704

Program and phase

SBIR · Phase I

Award year

1983

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
Not reported
Recipient company
Imr+e Corpon
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

THE OBJECTIVE OF THE PROPOSED RESEARCH IS TO DEVELOP AN IMMUNOLOGICALLY SPECIFIC ADSORBENT FOR USE IN EXTRACORPOREALSYSTEMS TO REMOVE IMMUNOREACTIVE IGM FROM THE SERUM OF PATIENTS FOR PRIMARY BILIARY CIRRHOSIS (PBC). BY STANDARD IMMUNOLOGIC TECHNIQUES, ANTIBODIES TO HUMAN IGM WILL BE ISOLATED. THESE ANTIBODIES WILL BE COVALENTLY LINKED TO SILICA TO PRODUCE A SPECIFIC IMMUNOADSORBENT. THIS ADSORBENT WILL BE TESTED "IN VITRO" IN A PHASE I STUDY TO ASSESS THE QUANTITATIVE REMOVAL OF IGM AND IMMUNOREACTIVE IGM FROM NORMAL AND PATHOLOGIC SERA, RESPECTIVELY. IF EFFICACIOUS, THEN IGM WILL BE ISOLATED FROM NORMAL HUMAN SERUM AND MONOCLONAL ANTIBODIES TO THIS IGM WILL BE PRODUCED. THE MONOCLONAL ANTIBODY WILL BE COVALENTLY LINKEDTO SILICA, AND TESTED "IN VITRO" AS DESCRIBED ABOVE. UPON THE "IN VITRO" DEMONSTRATION OF QUANTITATIVE AND SPECIFIC REMOVAL OF IMMUNOREACTIVE IGM FROM THE PATHOLOGIC SERA, IMMUNOADSORBENT COLUMNS (HOUSED IN DISPOSABLE CARTRIDGES) WILL BE DEVELOPED FOR USE IN A PHASE II "IN VIVO" STUDY WHICH WILL ASSESS THE EFFECT OF SUCH TREATMENTS WHEN APPLIED TO PATIENTS WITH PBC. THIS "IN VIVO" STUDY (PHASE II) WILL PROVIDE EVIDENCE FOR THE EFFICACY OF THIS APPROACH IN REMOVING IMMUNOREACTIVE IGM. PRESENT EVIDENCE SUGGESTS THAT THE IGM FROM PBC PATIENTS MAY BEHAVE LIKE AN IMMUNE COMPLEX, ALTHOUGH IT HAS THE SAME PHYSICAL-CHEMICAL PROPERTIES AS NORMAL IGM. WHEN FEASIBLE, A LONG TERM STUDY WILL ALLOW ASSESSMENT OF WHETHER THIS SPECIFIC IMMUNOADSORBENT EXTRACORPOREAL TECHNIQUE WILL ALTER THE NATURAL HISTORY OF THE DISEASE. CURRENTLY THERE IS NO SPECIFIC TREATMENT FOR PBC, AND ITS NATURAL COURSE, ALTHOUGH VARIABLE, TENDS TO BE PROGRESSIVE, LEADING TO DEATH IN TEN TO FIFTEEN YEARS. FROM THIS PROPOSED RESEARCH PLAN, IT IS ANTICIPATED THAT A BIOLOGICALLY SPECIFIC EXTRACORPOREAL IMMUNOADSORBENT WILL BE DEVELOPED WHICH WILL ALLOW PERIODIC REMOVAL OF IMMUNOREACTIVE IGM FROM PATIENTS SERA RESULTING IN IMPROVEMENT OF THEIR ALTERED IMMUNE STATE.IN ADDITION, IT IS ANTICIPATED THAT THIS SPECIFIC EXTRACORPOREAL APPROACH WILL BECOME COMMERCIALLY AVAILABLE, AND MAY BE EXTENDED TO OTHER "AUTOIMMUNE" DISORDERS WHERE ALTERED IMMUNE MECHANISMS ARE PRESUMED TO PLAY A ROLE IN PATHOGENESIS.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.