Difference between revisions of "Canine Leukocyte Adhesion Deficiency"

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Revision as of 22:22, 9 October 2010


Also known as: CLAD — Canine Granulocytopathy Syndrome

Introduction

Leucocyte adhesion deficiency (LAD) is caused by a defect in a surface molecule expressed by neutrophils which usually allows this type of cell to attach to vessel walls and move into tissues. The disease was first reported in a dog in 1987[1] and it bears similarities to leucocyte adhesion deficiencies in mice and humans. The surface molecule, the integrin subunit CD18, is affected by a mis-sense mutation of Cys-38-Ser and this results in a failure to express multiple integrin molecules as CD18 is a common subunit in several heterodimeric complexes. The disease is inherited in an autosomal recessive manner, with heterozygous carriers showing no signs of disease.

Since stimulatory cytokines are still released from inflamed tissues, neutrophils are produced in greater numbers from the bone marrow and released into the circulation. As these cells are unable to enter tissues, affected animals develop a persistent neutrophilia. Neutrophils from affected animals also show defects in chemotaxis and phagocytosis.

Signalment

The genetic defect described above has only been described in dogs of the Irish setter breed and in a very small number of Irish setter crosses[2].

Diagnosis

LAD is a very rare disease and should only be seriously considered in Irish setters with relevant genetic history.

Clinical Signs

Affected animals show signs of recurrent infections without neutrophilic exudates. Signs which have been described include[3]:

  • Pyrexia
  • Skin lesions including pyoderma, furunculosis and ulceration
  • Anorexia and failure to gain weight
  • Bone disorders including metaphyseal osteopathy, craniomandibular osteopathy and osteomyelitis
  • Generalised lymphadenopathy

Laboratory Tests

Haematological analysis of blood samples will reveal a persistent neutrophilia.

Other Tests

Genetic tests are now available to screen for the mutation in the CD18 gene in Irish setters[4]. Carrier animals can then be prevented from breeding in future. A study of Irish setters in Germany revealed a carriage rate of 11%[5].

Treatment

Supportive therapy may be attempted with antibiotics for specific infections but this is associated with a poor success rate.

More recently, various forms of stem cell therapy have been attempted to introduce cells capable of expressing CD18. Typically, CD34 positive (pluripotential) stem cells are transformed with a viral vector expressing CD18 before being transfused into puppies suffering from CLAD. The technique has achieved success when foamy virus or gamma retroviral vectors were used to transfect the stem cells[6][7].

Prognosis

Affected animals are unlikely to survive beyond six months of age as they are unable to control widespread bacterial infections.

Literature Search

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Canine Leukocyte Adhesion Deficiency publications

References

  1. Giger U, Boxer LA, Simpson PJ, Lucchesi BR, Todd RF 3rd. Deficiency of leukocyte surface glycoproteins Mo1, LFA-1, and Leu M5 in a dog with recurrent bacterial infections: an animal model. Blood. 1987 Jun;69(6):1622-30.
  2. Debenham SL, Millington A, Kijast J, Andersson L, Binns M. Canine leucocyte adhesion deficiency in Irish red and white setters. J Small Anim Pract. 2002 Feb;43(2):74-5.
  3. Trowald-Wigh G, Ekman S, Hansson K, Hedhammar A, Hård af Segerstad C. Clinical, radiological and pathological features of 12 Irish setters with canine leucocyte adhesion deficiency. J Small Anim Pract. 2000 May;41(5):211-7.
  4. Verfaillie T, Verdonck F, Cox E. Simple PCR-based test for the detection of canine leucocyte adhesion deficiency. Vet Rec. 2004 Jun 26;154(26):821-3.
  5. Pfeiffer I, Brenig B. Frequency of the canine leucocyte adhesion deficiency (CLAD) mutation among Irish red setters in Germany. J Anim Breed Genet. 2005 Apr;122(2):140-2.
  6. Hai M, Adler RL, Bauer TR Jr, Tuschong LM, Gu YC, Wu X, Hickstein DD. Potential genotoxicity from integration sites in CLAD dogs treated successfully with gammaretroviral vector-mediated gene therapy. Gene Ther. 2008 Jul;15(14):1067-71. Epub 2008 Mar 27.
  7. Bauer TR Jr, Allen JM, Hai M, Tuschong LM, Khan IF, Olson EM, Adler RL, Burkholder TH, Gu YC, Russell DW, Hickstein DD. Successful treatment of canine leukocyte adhesion deficiency by foamy virus vectors. Nat Med. 2008 Jan;14(1):93-7. Epub 2007 Dec 23.

Ettinger, S.J, Feldman, E.C. (2005) Textbook of Veterinary Internal Medicine (6th edition, volume 2) Saunders Elsevier