Medicine:WHIM syndrome
| WHIM syndrome | |
|---|---|
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| WHIM syndrome has an autosomal dominant pattern of inheritance. | |
| Specialty | Immunology |
| Symptoms | low red blood cells a higher risk of infections |
WHIM syndrome (or Warts, Hypogammaglobulinemia, Immunodeficiency, and Myelokathexis syndrome) is a rare congenital immunodeficiency disorder characterized by chronic noncyclic neutropenia.
Pathophysiology
WHIM syndrome results from autosomal dominant mutations in the gene for the chemokine receptor, CXCR4,[1][2] resulting in a carboxy-terminus truncation of the receptor of between 10 and 19 residues. The gene mutant is located on 2q21. The truncation of the receptor protein results in the inability of downregulation after stimulation. Thus, the receptor remain in an activated state.[3] WHIM syndrome is one of only a few diseases directly and primarily caused by an aberrant chemokine, making its molecular biology important in understanding the role of cell signaling and trafficking.[citation needed]
An association with GRK3 has also been observed.[4]
Diagnosis
Patients exhibit increased susceptibility to bacterial and viral infections, especially from common serotype human papilloma virus, resulting in warts on the hands and feet starting in childhood. Myelokathexis refers to retention (kathexis) of neutrophils in the bone marrow (myelo). In addition, lymphocytes and IgG antibody levels (gammaglobulins) are often deficient.[citation needed]
Treatment
Infusions of immune globulin can reduce the frequency of bacterial infections, and G-CSF or GM-CSF therapy improves blood neutrophil counts.[5]
As WHIM syndrome is a molecular disease arising from gain-of-function mutations in CXCR4, preclinical studies identified plerixafor, a specific CXCR4 antagonist, as a potential mechanism-based therapeutic for the disease.[6] Two subsequent clinical trials involving a handful of patients with WHIM syndrome demonstrated that plerixafor could increase white blood cell counts and continues to be a promising targeted therapy.[7][8]
A woman with spontaneous remission of her WHIM syndrome due to chromothripsis in one of her blood stem cells has been identified.[9][10]
In support of these studies, a 2014 phase I clinical trial treated three patients diagnosed with WHIM syndrome with plerixafor twice a day for six months. All three patients presented with multiple reoccurring infections before treatment and all had an increase in their white blood cell count post treatment. One patient (P3) had a decrease in his infections by 40% while the remaining two patients (P1 and P2) had no infections throughout the entirety of the treatment. Plerixafor may also prove to have anti-human papillomavirus (HPV) properties as all patients experienced a shrinkage or complete disappearance of their warts. While this treatment shows promise in treating neutropenia (decreased white blood cells), this trial showed no increase of immune globulins in the body.[11] A phase III clinical trial has been approved to compare the infection prevention ability of plerixafor versus the current treatment of G-CSF in patients with WHIM.[12]
References
- ↑ "Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease". Nat. Genet. 34 (1): 70–4. May 2003. doi:10.1038/ng1149. PMID 12692554.
- ↑ "WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4". Blood 109 (1): 78–84. January 2007. doi:10.1182/blood-2006-05-025296. PMID 16946301.
- ↑ "CXCR4 dimerization and beta-arrestin-mediated signaling account for the enhanced chemotaxis to CXCL12 in WHIM syndrome". Blood 112 (1): 34–44. July 2008. doi:10.1182/blood-2007-07-102103. PMID 18436740. https://hal-pasteur.archives-ouvertes.fr/pasteur-00284464/file/08-_15_-_Blood.pdf.
- ↑ "Leukocyte analysis from WHIM syndrome patients reveals a pivotal role for GRK3 in CXCR4 signaling". J. Clin. Invest. 118 (3): 1074–84. March 2008. doi:10.1172/JCI33187. PMID 18274673.
- ↑ "A new familial immunodeficiency disorder characterized by severe neutropenia, a defective marrow release mechanism, and hypogammaglobulinemia.". Am. J. Med. 89 (5): 663–72. 1990. doi:10.1016/0002-9343(90)90187-i. PMID 2239986.
- ↑ "AMD3100 is a potent antagonist at CXCR4(R334X), a hyperfunctional mutant chemokine receptor and cause of WHIM syndrome.". J. Cell. Mol. Med. 15 (10): 2071–81. 2011. doi:10.1111/j.1582-4934.2010.01210.x. PMID 21070597.
- ↑ "The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome.". Blood 118 (18): 4957–62. 2011. doi:10.1182/blood-2011-07-368084. PMID 21890643.
- ↑ "The CXCR4 antagonist plerixafor is a potential therapy for myelokathexis, WHIM syndrome.". Blood 118 (18): 4963–6. Nov 2011. doi:10.1182/blood-2011-06-360586. PMID 21835955.
- ↑ Kaiser, Jocelyn (5 February 2015). "Shattered chromosome cures woman of immune disease". Science. https://www.science.org/content/article/shattered-chromosome-cures-woman-immune-disease.
- ↑ David H. McDermott; Ji-Liang Gao; Qian Liu; Marie Siwicki; Craig Martens; Paejonette Jacobs; Daniel Velez; Erin Yim et al. (5 February 2015). "Chromothriptic Cure of WHIM Syndrome". Cell 160 (4): 686–699. doi:10.1016/j.cell.2015.01.014. ISSN 0092-8674. PMID 25662009.
- ↑ McDermott, David H.; Liu, Qian; Velez, Daniel; Lopez, Lizbeeth; Anaya-O’Brien, Sandra; Ulrick, Jean; Kwatemaa, Nana; Starling, Judy et al. (2014-04-10). "A phase 1 clinical trial of long-term, low-dose treatment of WHIM syndrome with the CXCR4 antagonist plerixafor" (in en). Blood 123 (15): 2308–2316. doi:10.1182/blood-2013-09-527226. ISSN 0006-4971. PMID 24523241.
- ↑ "Plerixafor Versus G-CSF in the Treatment of People With WHIM Syndrome - Full Text View - ClinicalTrials.gov" (in en). https://clinicaltrials.gov/ct2/show/NCT02231879.
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