Recent studies of cartilage-hair hypoplasia (CHH), a form of short-limbed dwarfism, have shown that all affected individuals have a cellular proliferation defect that results in a cellular immunodeficiency. However, only a minority of CHH individuals suffer from severe, life-threatening infections. For this reason, relevant immune defense mechanisms that may be responsible for maintaining intact host defenses in the majority of CHH individuals were studied. Spontaneous and allogeneic culture-induced (mixed lymphocyte response-MLR) specific and nonspecific (NK-like) cytotoxic mechanisms were analyzed and correlated with lymphocyte subpopulations present in CHH and normal individuals. Spontaneous natural-killer (NK) activity was present at or above normal levels, but culture-induced specific cytotoxicity and NK-like cytotoxicity as well as NK-like activity by T cell lines were significantly reduced in CHH individuals. The generation of radiation-resistant cytotoxicity, which normally occurs during allogeneic MLR, was markedly diminished in CHH, and was correlated with the decreased proliferation observed in CHH cultures. Preservation of spontaneous NK activity and loss of all forms of culture-induced cytotoxicity was associated with an increase in the proportion of lymphocytes bearing a thymic independent NK phenotype (OKM1+ OKT3- Fc gamma + low-affinity E+), and a significant decrease in thymic derived OKT3+ cytolytic T cell sub-populations in CHH individuals. Therefore, an intact cellular cytotoxic effector mechanism has been identified in CHH (i.e., NK activity). Natural cytotoxicity may be of importance in maintaining host resistance to viral infections despite diminished thymic-derived effector mechanisms in cartilage-hair hypoplasia.
G F Pierce, C Brovall, B Z Schacter, S H Polmar
Title and authors | Publication | Year |
---|---|---|
Immunologic and clinical features of 25 Amish patients with RMRP 70 A→G cartilage hair hypoplasia
NL Rider, DH Morton, E Puffenberger, CL Hendrickson, DL Robinson, KA Strauss |
Clinical Immunology | 2009 |
Immunodeficiency as a component of recognizable syndromes
JE Ming, ER Stiehm, JM Graham |
American Journal of Medical Genetics | 1996 |
Cartilage-hair hypoplasia — clinical manifestations in 108 Finnish patients
O Mäkitie, I Kaitila |
European Journal of Pediatrics | 1993 |
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: Description of seven patients and review of the literature
IV der Burgt, A Haraldsson, JC Oosterwijk, AJ van Essen, C Weemaes, B Hamel |
American Journal of Medical Genetics | 1991 |
Long-term immunological reconstitution by peripheral blood leucocytes in severe combined immune deficiency disease: implications for the role of mature lymphocytes in histocompatible bone marrow transplantation
SH Polmar, BZ Schacter, RU Sorensen |
Clinical & Experimental Immunology | 1986 |
Late-onset rubella syndrome: coexistence of immune complex disease and defective cytotoxic effector cell function
H Verder, E Dickmeiss, S Haahr, E Kappelgaard, J Leerbøy, A Møller-Larsen, H Nielsen, P Platz, C Koch |
Clinical & Experimental Immunology | 1986 |
Natural cytotoxicity in immunodeficiency diseases: Preservation of natural killer activity and the in vivo appearance of radioresistant killing
GF Pierce, SH Polmar, BZ Schacter, C Brovall, DL Hornick, RU Sorensen |
Human Immunology | 1986 |
Cartilage hair hypoplasia: Immunological aspects and their clinical implications
SH Polmar, GF Pierce |
Clinical Immunology and Immunopathology | 1986 |
Intestinal lymphangiectasia and thymic hypoplasia
RU Sorensen, TC Halpin, CR Abramowsky, DL Hornick, KM Miller, P Naylor, GS Incefy |
Clinical & Experimental Immunology | 1985 |