[CIS PIDD] [cis-pidd] Test for OKT4 epitope deficiency

CIS-PIDD cis-pidd at lists.clinimmsoc.org
Mon Oct 24 17:43:42 EDT 2016


What are his percent CD3+ and CD8+ of his TCR+ cells?…you should be able to do the math to see if he has CD4 cells.  Also…was class II measured?  Does the lab you sent it to have other CD4 clones available?

Best

James


James W. Verbsky M.D./Ph.D.
Associate Professor of Pediatrics and Microbiology
Medical Director, Clinical Immunology Research Laboratory
Medical Director, Clinical and Translational Research
Medical College of Wisconsin
Milwaukee, WI





From: CIS-PIDD [mailto:cis-pidd at lists.clinimmsoc.org]
Sent: Monday, October 24, 2016 3:33 PM
To: CIS-PIDD
Subject: [cis-pidd] Test for OKT4 epitope deficiency

Dear Professors,

I follow a patient whom I would like to test for OKT4 epitope deficiency. Does any lab perform this test in the US?
The patient is a 2yo male who presented with severe autoimmune aplastic anemia and was found to have severe CD4 lymphopenia (other lymphocyte subsets are normal) and asymptomatic CMV viremia. Infection history is otherwise unremarkable and patient otherwise appears healthy. HIV and TB tests are negative. He had low response to PHA and ConA and normal response to Pokeweed. IgG is nl, IgM is slightly low. He got IVIG back in July before I was consulted, I haven't gotten vaccine titers.
Aplastic anemia did not improve once CMV viral load became negative s/p treatment with valacyclovir.
I'm considering sending SCID genetic panel on this patient as well.

Thank you,

Araceli

Araceli Elizalde, MD
Immunology Clinic Director
Assistant Professor of Clinical Pediatrics
Allergy, Immunology & Rheumatology
Children's Hospital of San Antonio
Baylor College of Medicine


-----Original Message-----
From: CIS-PIDD <cis-pidd at lists.clinimmsoc.org<mailto:cis-pidd at lists.clinimmsoc.org>>
To: CIS-PIDD <cis-pidd at lyris.dundee.net<mailto:cis-pidd at lyris.dundee.net>>
Sent: Fri, Oct 21, 2016 5:37 pm
Subject: [cis-pidd] Steroid-responsive Dysuria in CGD
Colleagues:

I follow an 18 month old boy with X-CGD.  He seems to have dysuria that is responsive within a day or two to systemic steroids.  He has had a normal procto-colonoscopy and most recently normal cystoscopy with biopsies negative for inflammation and with no visual evidence of obstruction in the lower urinary tract.

What am I missing?

Joe Church
Children’s Hospital Los Angeles

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