Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Fall;3(2):e94-7.
doi: 10.2500/ar.2012.3.0035. Epub 2012 Dec 13.

Signal transducer and activator of transcription 3 mutation with invasive eosinophilic disease

Affiliations

Signal transducer and activator of transcription 3 mutation with invasive eosinophilic disease

Kara Crosby et al. Allergy Rhinol (Providence). 2012 Fall.

Abstract

Hyper-IgE syndrome (HIES), or Jobs disease, is a rare immunologic disorder characterized by the triad of staphylococcal abscesses, pneumonia with pneumatocele formation, and elevated IgE. It has been shown to have multiple modes of inheritance, autosomal dominant being more common than autosomal recessive, with sporadic cases as well. A mutation in signal transducer and activator of transcription 3 (STAT3) gene has been linked to the development of the sporadic and dominant forms of HIES. Peripheral eosinophilia, typically greater than two standard deviations from the normal population, is often seen in association with HIES. Despite these elevated levels of blood eosinophils, there have been no reported cases of invasive eosinophilic disease, such as eosonophilic esophagitic. Here we report the first description, to our knowledge, of a patient with HIES with a STAT3 mutation involving exon 12, Thr389Ile, and invasive eosinophilic disease of the esophagus. STAT3 modulates the expression of several genes that control central cell processes such as growth and death in response to external soluble stimuli. A mutation in the STAT3 molecule may affect the eosinophil's response to IL-5 and thus reduce the chemotaxic ability of those cells to migrate into tissues. This may then explain the paucity of eosinophilic infiltrative disease in patients with STAT3 mutations. The level of eosinophilic involvement may be related to the site or type of mutation within the STAT3 molecule. As more data are collected, we may be able to assess whether certain mutations dictate different clinical outcomes, which could prove helpful in directing therapy.

Keywords: Eosinophilia; STAT3; Thr389Ile; esophagitis; hyper-IgE; immunodeficiency; invasive.

PubMed Disclaimer

Conflict of interest statement

The authors have no conflicts of interest to declare pertaining to this article

Figures

Figure 1.
Figure 1.
Esophagogastroduodenoscopy (EGD) shows mucosal changes that include a ringed esophagus in the middle third of the esophagus.
Figure 2.
Figure 2.
Biopsy specimen from the middle third of the esophagus. Examination of the squamous epithelium shows an increased number of eosinophils; with an average of 20 eosinophils/high-powered field (HPF) and focal areas of 60 eosinophils/HPF.

Similar articles

Cited by

References

    1. Grimbacher B, Holland SM, Gallin JI, et al. Hyper-IgE syndrome with recurrent infections—An autosomal dominant multisystem disorder. N Engl J Med 340:692–702, 1999. (PubMed PMID: 10053178.) - PubMed
    1. National Institutes of Health Table 1. Scoring system with clinical and laboratory tests for individuals in kindreds with HIES. Available online at www.niaid.nih.gov/LabsAndResources/labs/aboutlabs/lcid/stat3base/Documen...; accessed August 6, 2012
    1. Farkas L. Anthropometry of the head and face. 2nd ed New York, NY: Raven Press; 286–301, 1994
    1. Zhang Q, Davis JC, Lamborn IT, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med 361:2046–2055, 2009. (PubMed PMID: 19776401.) - PMC - PubMed
    1. Grimbacher B, Holland SM, Puck JM. Hyper-IgE syndromes. Immunol Rev 203:244–250, 2005. (PubMed PMID: 15661034.) - PubMed