Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century
Peter D. Arkwright
Department of Paediatric Allergy and Immunology, Royal Manchester Children's Hospital, University of Manchester, Manchester, United Kingdom.
Search for more papers by this authorAndrew R. Gennery
Department of Paediatric Immunology, University of Newcastle upon Tyne, Newcastle, United Kingdom
Search for more papers by this authorPeter D. Arkwright
Department of Paediatric Allergy and Immunology, Royal Manchester Children's Hospital, University of Manchester, Manchester, United Kingdom.
Search for more papers by this authorAndrew R. Gennery
Department of Paediatric Immunology, University of Newcastle upon Tyne, Newcastle, United Kingdom
Search for more papers by this authorPreferred citation: Arkwright, P.D. & A.R. Gennery. 2011. Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century. In “The Year in Human and Medical Genetics: Inborn Errors of Immunity I.” Jean-Laurent Casanova, Mary Ellen Conley & Luigi Notarangelo, Eds. Ann. N.Y. Acad. Sci. 1238: 7–14.
Abstract
The 10 warning signs of primary immunodeficiency are being promoted as a screening tool for use by both the general public and physicians. A recent study, however, shows that except for family history, need for intravenous antibiotics and failure to thrive, the 10 warning signs are not a useful screen of primary immunodeficiency diseases (PIDs). Over the last few decades, there has been a revolution in our understanding of PID. The 10 warning signs do not take into account the fact that PIDs now include diseases that present with sporadic infections, autoimmunity, autoinflammation, and malignancy. This review focuses on the advances in our understanding of PID, the current limitations of the 10 warning signs, and recommendations to ensure that patients with PID are diagnosed in a timely fashion in the future.
References
- 1
Cohn, E.J.,
J.L. Oncley,
L.E. Strong,
et al
. 1944. Chemical, clinical, and immunological studies on the products of human plasma fractionation. I. The characterization of the protein fractions of human plasma.
J. Clin. Invest.
23: 417–432.
- 2
Geha, R.S.
2005. Charles A. Janeway and Fred S. Rosen: the discovery of gamma globulin therapy and primary immunodeficiency diseases at Boston Children's Hospital.
J. Allergy Clin. Immunol.
116: 937–940.
- 3
Gesner, B.M. &
J.L. Gowans. 1962. The fate of lethally irradiated mice given isologous and heterologous thoracic duct lymphocytes.
Br. J. Exp. Pathol.
43: 431–440.
- 4
Berendes, H.,
R.A. Bridges &
R.A. Good. 1957. A fatal granulomatosus of childhood: the clinical study of a new syndrome.
Minn. Med.
40: 309–312.
- 5
Donohue, W.L.
1953. Alymphocytosis.
Pediatrics
11: 129–139.
- 6
Aldrich, R.A.,
A.G. Steinberg &
D.C. Campbell. 1954. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.
Pediatrics
13: 133–139.
- 7
Bruton, O.C.
1953. Agammaglobulinemia (congenital absence of gamma globulin); report of a case.
Med. Ann. Dist. Columbia.
22: 648–650.
- 8
Thomas, E.D.,
H.L. Lochte &
J.W. Ferrebee. 1959. Irradiation of the entire body and marrow transplantation: some observations and comments.
Blood
14: 1–23.
- 9
Cunningham-Rundles, C. &
C. Bodian. 1999. Common variable immunodeficiency: clinical and immunological features of 248 patients.
Clin. Immunol.
92: 34–48.
- 10
Plebani, A.,
A. Soresina,
R. Rondelli,
et al
. 2002. Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study.
Clin. Immunol.
104: 221–230.
- 11
Winkelstein, J.A.,
M.C. Marino,
H.M. Lederman,
et al
. 2006. X-linked agammaglobulinemia: a report on a United States registry of 201 patients.
Medicine
85: 193–202.
- 12
Marodi, L. &
J.L. Casanova. 2009. Primary immunodeficiency diseases: the J Project.
Lancet
373: 2179–2181.
- 13
Marodi, L. &
J.L. Casanova. 2009. Novel primary immunodeficiencies relevant to internal medicine: novel phenotypes.
J. Intern. Med.
266: 502–506.
- 14
Spickett, G.P.,
S.A. Misbah &
H.M. Chapel. 1991. Primary antibody deficiency in adults.
Lancet
337: 281–284.
- 15
Subbarayan, A.,
G. Colarusso,
S.M. Hughes,
et al
. 2011. Clinical features that identify children with primary immunodeficiency diseases.
Pediatrics
127: 810–816.
- 16
Picard, C.,
H. von Bernuth,
P. Ghandil,
et al
. 2010. Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency.
Medicine
89: 403–425.
- 17
Sancho-Shimizu, V.,
S.Y. Zhang,
L. Abel,
et al
. 2007. Genetic susceptibility to herpes simplex virus 1 encephalitis in mice and humans.
Curr. Opin. Allergy Clin. Immunol.
7: 495–505.
- 18
Casanova, J.L.,
L. Abel &
L. Quintana-Murci. 2011. Human TLRs and IL-1Rs in host defence: natural insights from evolutionary, epidemiological, and clinical genetics.
Annu. Rev. Immunol.
29: 447–491.
- 19
Casanova, J.L. &
L. Abel. 2007. Primary immunodeficiencies: a field in its infancy.
Science
317: 617–619.
- 20
Hoare, S.,
O. El-Shazali,
J.E. Clark,
et al
. 2002. Investigation for complement deficiency following meningococcal disease.
Arch. Dis. Child.
86: 215–217.
- 21
Pessach, I.,
J. Walter &
L.D. Notarangelo. 2009. Recent advances in primary immunodeficiencies: identification of novel genetic defects and unanticipated phenotypes.
Pediatr. Res.
65: 3R–12R.
- 22
Arason, G.J.,
G.H. Jorgensen &
B.R. Ludviksson. 2010. Primary immunodeficiency and autoimmunity: lessons from human diseases.
Scand. J. Immunol.
71: 317–328.
- 23
Fischer, A.
2007. Human primary immunodeficiency diseases.
Immunity
27: 835–845.
- 24
Bennett, C.L.,
J. Christie,
F. Ramsdell,
et al
. 2001. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
Nat. Genet.
27: 20–21.
- 25
Winkelstein, J.A.,
M.C. Marino,
R.B. Johnston, Jr.,
et al
. 2000. Chronic granulomatous disease. Report on a national registry of 368 patients.
Medicine
79: 155–169.
- 26
Bhat, A.,
S.M. Naguwa &
M.E. Gershwin. 2007. Genetics and new treatment modalities for familial Mediterranean fever.
Ann. N.Y. Acad. Sci. 1110: 201–208.
- 27
Rezaei, N.,
E. Mahmoudi,
A. Aghamohammadi,
et al
. 2011. X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma.
Br. J. Haematol.
152: 13–30.
- 28
Huck, K.,
O. Feyen,
T. Niehues,
et al
. 2009. Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.
J. Clin. Invest.
119: 1350–1358.
- 29
Slatter, M.A. &
A.R. Gennery. 2010. Primary immunodeficiency syndromes.
Adv. Exp. Med. Biol.
685: 146–165.
- 30
The International Nijmegen Breakage Syndrome Study Group. 2000. Nijmegen breakage syndrome.
Arch. Dis. Child.
82: 400–406.
- 31
De Benedetto, A.,
R. Agnihothri,
L.Y. McGirt,
et al
. 2009. Atopic dermatitis: a disease caused by innate immune defects?
J. Invest. Dermatol.
129: 14–30.
- 32
Ong, P.Y. &
D.Y. Leung. 2010. The infectious aspects of atopic dermatitis.
Immunol. Allergy Clin. North Am.
30: 309–321.
- 33
Schroder, J.M.
2010. The role of keratinocytes in defense against infection.
Curr. Opin. Infect. Dis.
23: 106–110.
- 34
Hammad, H. &
B.N. Lambrecht. 2011. Dendritic cells and airway epithelial cells at the interface between innate and adaptive immune responses.
Allergy
66: 579–587.
- 35
Liu, Y.J.
2006. Thymic stromal lymphopoietin: master switch for allergic inflammation.
J. Exp. Med.
203: 269–273.
- 36
Ziegler, S.F. &
D. Artis. 2010. Sensing the outside world: TSLP regulates barrier immunity.
Nat. Immunol.
11: 289–293.
- 37
Baker, B.S.
2006. The role of microorganisms in atopic dermatitis.
Clin. Exp. Immunol.
144: 1–9.
- 38
Palmer, C.N.,
A.D. Irvine,
A. Terron-Kwiatkowski,
et al
. 2006. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.
Nat. Genet.
38: 441–446.
- 39
O’Regan, G.M.,
A. Sandilands,
W.H. McLean &
A.D. Irvine. 2008. Filaggrin in atopic dermatitis.
J. Allergy Clin. Immunol.
122: 689–693.
- 40
Thyssen, J.P.,
B.C. Carlsen,
T. Menné,
et al
. 2010. Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study.
Br. J. Dermatol.
163: 115–120.
- 41
Weidinger, S.,
M. O'Sullivan,
T. Illig,
et al
. 2008. Filaggrin mutations, atopic eczema, hay fever, and asthma in children.
J. Allergy Clin. Immunol.
121: 1203–1209.
- 42
Howell, M.D.,
B.E. Kim,
P. Gao,
et al
. 2009. Cytokine modulation of atopic dermatitis filaggrin skin expression.
J. Allergy Clin. Immunol.
124(Suppl. 2): R7–R12.
- 43
Gao, P.S.,
N.M. Rafaels,
T. Hand,
et al
. 2009. Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum.
J. Allergy Clin. Immunol.
124: 507–513.
- 44
Gennery, A.R.
2006. Primary immunodeficiency syndromes associated with defective DNA double-strand break repair.
Br. Med. Bull.
77–78: 71–85.
- 45
Meyer, B.F.
2005. Strategies for the prevention of hereditary diseases in a highly consanguineous population.
Ann. Hum. Biol.
32: 174–179.
- 46
Zlotogora, J.
2009. Population programs for the detection of couples at risk for severe monogenic genetic diseases.
Hum. Genet.
126: 247–253.
- 47
Bittles, A.H.
2008. A community genetics perspective on consanguineous marriage.
Community Genet.
11: 324–330.
- 48
Modell, B. &
A. Darr. 2002. Science and society: genetic counselling and customary consanguineous marriage.
Nat. Rev. Genet.
3: 225–229.
- 49
Routes, J.M.,
W.J. Grossman,
J. Verbsky,
et al
. 2009. Statewide newborn screening for severe T-cell lymphopenia.
JAMA
302: 2465–2470.
- 50
Comeau, A.M.,
J.E. Hale,
S.Y. Pai,
et al
. 2010. Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency.
J. Inherit. Metab. Dis.
33(Suppl. 2): S273–S281.