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
Review
. 2021 Mar 5;21(3):14.
doi: 10.1007/s11882-020-00984-8.

Disease Presentation, Treatment Options, and Outcomes for Myeloid Immunodeficiencies

Affiliations
Review

Disease Presentation, Treatment Options, and Outcomes for Myeloid Immunodeficiencies

Elizabeth M Kang. Curr Allergy Asthma Rep. .

Abstract

Purpose of review: Up-to-date review on various types of immunodeficiencies with a significant myeloid component including some more recently described congenital disorders.

Recent findings: While a number of disorders have been described in the past, genetic sequencing has led to the identification of the specific disorders and clarified their pathophysiology. Advances in genetic therapies including genetic editing should provide future treatments beyond hematopoietic stem cell transplant for patients with these rare disorders. Neutrophils (or granulocytes) are a major contributor to infection surveillance and clearance, and defective neutrophils characteristically lead to pyogenic infections. Deficiency in numbers, either iatrogenic or congenital; functional defects; and/or inability to target to the sites of infection can all lead to serious morbidity and mortality; however, myeloid-based immunodeficiencies are not all the same. Having absent neutrophils, that is, neutropenia, has implications different to those of having dysfunctional neutrophils as will become evident as the various disorders are reviewed.

Keywords: Gene therapy; Immunodeficiencies; Myeloid defects; Transplantation.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest

The authors declare no conflicts of interest relevant to this manuscript.

References

    1. Picard C, von Bernuth H, Ghandil P, et al. Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. Medicine (Baltimore) 2010; 89: 403–425. 2010/November/09. DOI: 10.1097/MD.0b013e3181fd8ec3. - DOI - PMC - PubMed
    1. Ku CL, von Bernuth H, Picard C, et al. Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity. J Exp Med 2007; 204: 2407–2422. 2007/September/26. DOI: 10.1084/jem.20070628. - DOI - PMC - PubMed
    1. Gokturk B, Casanova JL, Picard C, et al. A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma. J Investig Allergol Clin Immunol 2018; 28: 271–273. 2018/August/04. DOI: 10.18176/jiaci.0261. - DOI - PubMed
    1. Platt CD, Zaman F, Wallace JG, et al. A novel truncating mutation in MYD88 in a patient with BCG adenitis, neutropenia and delayed umbilical cord separation. Clin Immunol 2019; 207: 40–42. 2019/July/14. DOI: 10.1016/j.clim.2019.07.004. - DOI - PMC - PubMed
    1. Hayward AR, Harvey BA, Leonard J, et al. Delayed separation of the umbilical cord, widespread infections, and defective neutrophil mobility. Lancet 1979; 1: 1099–1101. 1979/May/26. DOI: 10.1016/s0140-6736(79)91786-0. - DOI - PubMed

Publication types

MeSH terms

LinkOut - more resources