Important Mammalian Respiratory Allergens Are Lipocalins

Allergy is an expanding problem in the industrialized countries. Allergenic proteins, the allergens, causing the allergic symptoms are ubiquitous materials in the environment, normally not harmful for individuals not sensitized to them. In contrast, sensitized individuals who have specific immunoglobulin E against the allergen as a result of activation of the immune system can develop immediate, even fatal allergic reactions. Sensitization to indoor allergens, for example to those derived from pets, is often associated with more severe forms of allergic diseases, such as asthma. Recent years have shown that the major mammalian allergens causing respiratory sensitization belong to the lipocalin family of proteins. Reasons for this remain to be fully elucidated but it appears that lipocalin allergens exhibit immunological features that may account for their allergenic capacity.

Introduction

Allergy is a disorder of the immune system which is manifested as inappropriate reactions to ubiquitous materials in the environment such as pollen, house dust mites, or animal dander.¹ Allergic reactions are mediated by immunoglobulin E (IgE) antibody. Proteins able to bind IgE are called allergens. They initiate allergic or type I hypersensitivity reactions by cross-linking the antibody on mast cells and basophils. This results in the release of inflammatory mediators and in the symptoms of allergy. Allergic symptoms can arise from different organs, typically from airways, digestive track, and skin. Their severity varies, e.g., from mild rhinitis and itching to a systemic anaphylactic shock. Sensitization, as indicated by the presence of IgE, can be evaluated by measuring serum IgE or by skin prick tests (SPT). Sensitization can also develop without leading to a clinical illness.

The nomenclature of allergens is based on the system introduced by the Allergen Nomenclature Sub-Committee of the International Union of Immunological Societies.^2,3 The designation comprises the first three letters of the genus of origin of the allergen, the first letter of the species name, and a running Arabic number. If two species names have identical designations they are distinguished by adding one or more letters, as necessary, to each species designation. Isoallergens sharing an amino acid identity of ≥ 67% are distinguished by a two-digit number after the sequential number of the allergen and the variants with an additional two-digit number. For example, bovine dander allergen Bos d 2.0101 is the variant 01 of the isoallergen 01 of Bos d 2.

Exposure and Sensitization to Animal Allergens

The major respiratory allergens of animals (Table 1), especially from mammals, belong to the lipocalin family of proteins.^4,5 While the cat allergen Fel d 1 is an important exception to the rule (see refs. 6,7), another major cat allergen, Fel d 4, was recently reported to be a lipocalin.⁸ The food allergen Bos d 5 (β-lactoglobulin) also belongs to lipocalins.⁵

Household pets, cats and dogs, are frequently found in homes in the industrialized countries. As the allergens which emanate from these animals tend to stick to clothing, they are commonly found in other indoor environments, such as homes without pets, schools, day care centers, and transport vehicles. The concentrations may be high enough to sensitize and to cause symptoms in sensitized individuals.⁹ Assessed by skin prick tests (SPT), dogs sensitize 7-15% of individuals in community populations.^10,11 The figure can rise up to 56% among asthmatic children.¹² Among dog-allergic subjects, sensitization to Can f 1 is detected in 50-70% of the individuals (see refs. 13-15) while the figure for Can f 2 is about 25%.^14,15 The prevalence of sensitization to cat among children with asthma is 30-50%.^16,17 The predominant cat allergen Fel d 1, not a lipocalin, sensitizes over 90% of cat-allergic individuals.¹⁸ Sixty-three percent of cat-allergic individuals had IgE against Fel d 4, a recently discovered lipocalin allergen, typically at low levels.⁸

Exposure to rodents and to rabbit is a major occupational health problem since 20-30% of workers in laboratory animal facilities become sensitized to animal allergens.^19,20 Allergy to rabbit was observed to develop rapidly in laboratory animal workers, as its prevalence was the highest in comparison with sensitization to other animal species within one year of exposure.¹⁹ Sixty-six percent of laboratory workers with asthma and rhinitis had IgE against rat Rat n 1.²¹ In a survey of asthma patients, 35% of them had a positive SPT result with a rabbit dander extract.²² Mice, rats, hamsters, guinea pigs, and gerbils are popular pets, but mouse can also induce allergy in subjects who live in infested apartments. The prevalence of sensitization to mouse was 18% among inner-city children with asthma in a U.S. study.²³ Keeping guinea pigs was associated with a more than threefold risk for atopic eczema in comparison with having other pets, such as dogs, cats, or hamsters.²⁴ Seventy to 87% of guinea pig-allergic subjects had IgE reactivity to Cav p 1 while the reactivity to Cav p 2 was about 55%.²⁵

Domestic animals able to induce allergy include horse and cow. A population study reported a prevalence of about 13% for a positive SPT with horse dander.¹¹ Two of the characterized horse allergens, Equ c 1 and Equ c 2, are lipocalins. Seventy-six per cent of horse-allergic subjects had IgE to Equ c 1 (see ref. 26) while up to 50% had IgE against Equ c 2.²⁷ Cow epithelium is a potent sensitizer in the farming environment, inducing a variety of symptoms including asthma.²⁸ About 90% of dairy farmers with asthma of bovine origin have IgE against the major respiratory allergen of cow, Bos d 2.²⁹

Lipocalin allergens have also been detected in insects. Exposure to cockroach allergens depends on socioeconomic factors including housing conditions. Sensitization to cockroach is around 40% among inner-city children with asthma.³⁰ Forty to sixty per cent of asthmatic patients with cockroach allergy had IgE to recombinant Bla g 4, a lipocalin allergen.³¹ Another insect-derived lipocalin allergen is Tria p 1 from the “kissing bug”.³²

Immunological Features of Lipocalin Allergens

Although allergens bind IgE by definition, it is basically unknown why the inert environmental substances elicit the process of sensitization, the generation of T helper type 2 (Th2) lymphocytes, which results in the synthesis of allergen-specific IgE by B lymphocytes.^33,34 One requirement for a protein to be an allergen is that it is effectively dispersed in the environment. As discussed above, lipocalin allergens are widely encountered in human environments, obviously a result from the fact that lipocalin allergens are present in the dander and excretions of mammals. Another possible factor promoting the allergenic capacity of a protein could be its biological function. Lipocalins are known to exhibit a variety of biological functions (see ref. 35), including an enzyme activity (see ref. 36), which has been suggested to account for the allergenicity of some mite, fungal and pollen allergens.³⁷ The dog allergen Can f 1 has been proposed to be a cysteine protease inhibitor since it exhibits a considerable level of homology with tear lipocalin.³⁸ It can be speculated that like the allergens with enzyme activity (see ref. 37), lipocalin allergens might initially affect cell populations other than the T helper (Th) cells (lymphocytes), the crucial cell population in sensitization. For example, microbial pathogens can deliver signals to dendritic cells through pathogen-associated molecular patterns (PAMPs).³⁹ These signals can result in the polarization of T cell response, but lipocalins, or allergens in general, are not known to contain PAMPs. One endogenous lipocalin, glycodelin, acts on T cells directly. By elevating T cell receptor activation thresholds, glycodelin appears to favor the Th2 deviation of immune response.^40,41 Nevertheless, lipocalins are not known to possess a unifying physicochemical property or biological function which could explain their allergenicity.

Since Th cells play a central role in the specific immune response against exogenous substances and are therefore important in sensitization, it is possible that they are involved in determining the allergic capacity of proteins.^4,34 When we studied the cellular response against Bos d 2 we observed unexpectedly that the peripheral blood mononuclear cells (PBMC) from highly allergic cow dust-asthmatic patients with positive skin prick test reactions to Bos d 2 proliferated very weakly in vitro upon stimulation with the allergen.⁴² We have recently verified that the finding was not characteristic for Bos d 2 only since recombinant dog Can f 1 and horse Equ c 1 were also weak stimulants for the PBMCs of dog and horse-allergic patients, respectively (Tuomas Virtanen, to be published). Accordingly, rat Rat n 1 was reported to be weakly stimulatory in vitro.⁴³ In a study with murine cells, we found that Bos d 2 was a weak immunogen for several inbred mouse strains.⁴⁴ Our recent study suggests that the weak stimulatory capacity of lipocalin allergens can result from their poor recognition by Th cells since the immunodominant T cell epitope of Bos d 2 was observed to be suboptimal for human T cells.⁴⁵ The finding is interesting because a weak stimulation through T cell receptor is known to favor Th2-type responses.^46,47 As lipocalins can exhibit considerable amino acid identity between species, it can be speculated that the presence of endogenous lipocalins could have resulted in the deletion of high-avidity lipocalin allergen-reactive T cells during thymic maturation.^4,48 Consequently, the remaining T cell population might recognize exogenous lipocalin allergens weakly, promoting the Th2 deviation of immune response.

IgE antibodies cross-reactive between different allergens can result in symptoms in an individual who encounters an allergen which is able to bind the cross-reactive antibodies but was not their initial inducer. The cross-reactivity of IgE antibodies between non-serum-derived mammalian allergens is poorly known. At the level of allergen extracts, there seems to be cross-reactivity.^49,50 It has also been suggested that the major cat and dog allergens have common IgE epitopes.⁴⁹ In a study with guinea-pig Cav p 1, a 100-fold excess of cat, mouse, and rat allergen preparations were able to cause weak inhibition, less than 10%, in IgE ELISA, pointing to a low-level cross-reactivity.²⁵ A further study suggested that a part of the IgE-binding epitopes of Cav p 1 and 2 are also cross-reactive.⁵¹ Inhibition experiments with cow, dog and horse allergen extracts pointed to a possibility that cow dander contains a homolog with cat Fel d 4.⁸ Most probably it is not the bovine Bos d 2 (see below) since its amino acid identity with Fel d 4 is only 29% (SBNS, Dec. 9, 2004). A monoclonal antibody raised to Bos d 5 (β-lactoglobulin), a bovine food allergen, has been reported to react against human serum retinol-binding protein.⁵² The core of the epitope sequence, DTDY, is also found in glycodelin, another human lipocalin.

Mammalian Lipocalin Allergens Causing Respiratory Sensitization

Concluding Remarks

Allergenicity is a property shared by a number of animal lipocalins. Neither the molecular structure nor biologic activity has provided definite clues for the allergenicity of lipocalins. Allergenicity of a protein can be verified conclusively only immunologically, i.e., by showing its capacity to induce sensitization. We have proposed that the allergenicity of lipocalin allergens is related to the adaptation of the immune system to the presence of endogenous lipocalins. The weak capacity of lipocalin allergens to induce the proliferation of PBMCs and the suboptimal character of the immunodominant T cell epitope of Bos d 2 suggest that the recognition of a lipocalin allergen by Th cells can be involved in promoting the development of the Th2-deviated immune response. Although the mapping of T cell epitopes is a laborious process, on the practical level their identification may allow to design new modalities of allergen immunotherapy, based on natural or optimized allergen peptides.^81,82

Acknowledgements

The work was supported by Kuopio University Hospital (project # 5021605) and the Academy of Finland (contract # 205871).

References

1.

Janeway CAJ, Travers P, Walport M. et al. Allergy and hypersensitivity In: Immunobiology - The immune system in health and disease. 4th edNew York: Garland Publishing,2001471–500.

2.

King TP, Hoffman D, Løwenstein H. et al. Allergen nomenclature. Int Arch Allergy Immunol. 1994;105:224–233. [PubMed: 7920024]

3.

Chapman MD. Allergen nomenclatureIn: Lockey RF, Bukantz SC, Bousquet J, eds.Allergens and allergen immunotherapy. 3rd edNew York: Marcel Dekker, Inc.,200451–64.

4.

Virtanen T, Zeiler T, Rautiainen J. et al. Allergy to lipocalins: a consequence of misguided T-cell recognition of self and nonself? Immunol Today. 1999;20:398–400. [PubMed: 10462739]

5.

Åkerstrom B, Flower DR, Salier J-P. Lipocalins: unity in diversity. Biochim Biophys Acta. 2000;1482:1–8. [PubMed: 11058742]

6.

Morgenstern JP, Griffith IJ, Brauer AW. et al. Amino acid sequence of Fel d I, the major allergen of the domestic cat: protein sequence analysis and cDNA cloning. Proc Natl Acad Sci USA. 1991;88:9690–9694. [PMC free article: PMC52784] [PubMed: 1946388]

7.

Griffith IJ, Craig S, Pollock J. et al. Expression and genomic structure of the genes encoding FdI, the major allergen from the domestic cat. Gene. 1992;113:263–268. [PubMed: 1572548]

8.

Smith W, Butler AJ, Hazell LA. et al. Fel d 4, a cat lipocalin allergen. Clin Exp Allergy. 2004;34:1732–1738. [PubMed: 15544598]

9.

Munir AKM, Einarsson R, Schou C. et al. Allergens in school dust.1. The amount of the major cat (Fel d I) and dog (Can f I) allergens in dust from Swedish schools is high enough to probably cause perennial symptoms in most children with asthma who are sensitized to cat and dog. J Allergy Clin Immunol. 1993;91:1067–1074. [PubMed: 8491939]

10.

Haahtela T, Björksten F, Heiskala M. et al. Skin prick test reactivity to common allergens in Finnish adolescents. Allergy. 1980;35:425–431. [PubMed: 7192500]

11.

Barbee RA, Brown WG, Kaltenborn W. et al. Allergen skin-test reactivity in a community population sample: correlation with age, histamine skin reactions and total serum immunoglobulin E. J Allergy Clin Immunol. 1981;68:15–19. [PubMed: 7240595]

12.

Vanto T, Koivikko A. Dog hypersensitivity in asthmatic children. A clinical study with special reference to the relationship between the exposure to dogs and the occurrence of hypersensitivity symptoms. Acta Paediatr Scand. 1983;72:571–575. [PubMed: 6624434]

13.

Schou C, Svendsen UG, Løwenstein H. Purification and characterization of the major dog allergen, Can f I. Clin Exp Allergy. 1991;21:321–328. [PubMed: 1863894]

14.

Konieczny A, Morgenstern JP, Bizinkauskas CB. et al. The major dog allergens, Can f 1 and Can f 2, are salivary lipocalin proteins: cloning and immunological characterization of the recombinant forms. Immunology. 1997;92:577–586. [PMC free article: PMC1364166] [PubMed: 9497502]

15.

Saarelainen S, Taivainen A, Rytkönen-Nissinen M. et al. Assessment of recombinant dog allergens Can f 1 and Can f 2 for the diagnosis of dog allergy. Clin Exp Allergy. 2004;34:1576–1582. [PubMed: 15479273]

16.

Nelson HS, Szefler SJ, Jacobs J. et al. The relationships among environmental allergen sensitization, allergen exposure, pulmonary function, and bronchial hyperresponsiveness in the Childhood Asthma Management Program. J Allerg Clin Immunol. 1999;104:775–785. [PubMed: 10518821]

17.

Perzanowski MS, Ronmark E, Nold B. et al. Relevance of allergens from cats and dogs to asthma in the northernmost province of Sweden: schools as a major site of exposure. J Allergy Clin Immunol. 1999;103:1018–1024. [PubMed: 10359880]

18.

van ReeR, van LeeuwenWA, Bulder I. et al. Purified natural and recombinant Fel d 1 and cat albumin in in vitro diagnostics for cat allergy. J Allerg Clin Immunol. 1999;104:1223–1230. [PubMed: 10589005]

19.

Aoyama K, Ueda A, Manda F. et al. Allergy to laboratory animals: an epidemiological study. Br J Ind Med. 1992;49:41–47. [PMC free article: PMC1039233] [PubMed: 1733454]

20.

Bush RK, Wood RA, Eggleston PA. Laboratory animal allergy. J Allergy Clin Immunol. 1998;102:99–112. [PubMed: 9679853]

21.

Platts-Mills TA, Longbottom J, Edwards J. et al. Occupational asthma and rhinitis related to laboratory rats: serum IgG and IgE antibodies to the rat urinary allergen. J Allergy Clin Immunol. 1987;79:505–515. [PubMed: 3819230]

22.

Desjardins A, Benoit C, Ghezzo H. et al. Exposure to domestic animals and risk of immunologic sensitization in subjects with asthma. J Allergy Clin Immunol. 1993;91:979–986. [PubMed: 8491948]

23.

Phipatanakul W, Eggleston PA, Wright EC. et al. Mouse allergen. II. The relationship of mouse allergen exposure to mouse sensitization and asthma morbidity in inner-city children with asthma. J Allergy Clin Immunol. 2000;106:1075–1080. [PubMed: 11112889]

24.

Schäfer T, Heinrich J, Wjst M. et al. Indoor risk factors for atopic eczema in school children from East Germany. Environ Res. 1999;81:151–158. [PubMed: 10433847]

25.

Fahlbusch B, Rudeschko O, Szilagyi U. et al. Purification and partial characterization of the major allergen, Cav p 1, from guinea pig Cavia porcellus. Allergy. 2002;57:417–422. [PubMed: 11972481]

26.

Dandeu JP, Rabillon J, Divanovic A. et al. Hydrophobic interaction chromatography for isolation and purification of Equ.c1, the horse major allergen. J Chromatogr - Biomed Appl. 1993;621:23–31. [PubMed: 8308084]

27.

Bulone V, Krogstad-Johnsen T, Smestad-Paulsen B. Separation of horse dander allergen proteins by two-dimensional electrophoresis - Molecular characterisation and identification of Equ c 2.0101 and Equ c 2.0102 as lipocalin proteins. Eur J Biochem. 1998;253:202–211. [PubMed: 9578478]

28.

Zeiler T, Taivainen A, Mäntyjärvi R. et al. Threshold levels of purified natural Bos d 2 for inducing bronchial airway response in asthmatic patients. Clin Exp Allergy. 2002;32:1454–1460. [PubMed: 12372125]

29.

Ylönen J, Mäntyjärvi R, Taivainen A. et al. IgG and IgE antibody responses to cow dander and urine in farmers with cow-induced asthma. Clin Exp Allergy. 1992;22:83–90. [PubMed: 1551038]

30.

Rosenstreich DL, Eggleston P, Kattan M. et al. The role of cockroach allergy and exposure to cockroach allergen in causing morbidity among inner-city children with asthma. N Engl J Med. 1997;336:1356–1363. [PubMed: 9134876]

31.

Arruda LK, Vailes LD, Hayden ML. et al. Cloning of cockroach allergen, Bla g 4, identifies ligand binding proteins (or calycins) as a cause of IgE antibody responses. J Biol Chem. 1995;270:31196–31201. [PubMed: 8537384]

32.

Paddock CD, McKerrow JH, Hansell E. et al. Identification, cloning, and recombinant expression of procalin, a major triatomine allergen. J Immunol. 2001;167:2694–2699. [PubMed: 11509613]

33.

Blumenthal MN, Rosenberg A. Definition of an allergen (immunobiology)In: Lockey RF, Bukantz SC, Bousquet J, eds.Allergens and allergen immunotherapy. 3rd edNew York: Marcel Dekker, Inc.,200437–50. [PubMed: 15042907]

34.

Virtanen T, Mäntyjärvi R. Mammalian allergensIn: Lockey RF, Bukantz SC, Bousquet J, eds.Allergens and allergen immunotherapy. 3rd edNew York: Marcel Dekker, Inc.,2004297–317.

35.

Flower DR. The lipocalin protein family: structure and function. Biochem J. 1996;318:1–14. [PMC free article: PMC1217580] [PubMed: 8761444]

36.

Yusifov TN, Abduragimov AR, Gasymov OK. et al. Endonuclease activity in lipocalins. Biochem J. 2000;347:815–819. [PMC free article: PMC1221020] [PubMed: 10769187]

37.

Reed CE, Kita H. The role of protease activation of inflammation in allergic respiratory diseases. J Allergy Clin Immunol. 2004;114:997–1008. [PubMed: 15536399]

38.

Chapman MD, Wood RA. The role and remediation of animal allergens in allergic diseases. J Allergy Clin Immunol. 2001;107:S414–421. [PubMed: 11242602]

39.

Kapsenberg ML. Dendritic-cell control of pathogen-driven T-cell polarization. Nat Rev Immunol. 2003;3:984–993. [PubMed: 14647480]

40.

Rachmilewitz J, Riely GJ, Huang JH. et al. A rheostatic mechanism for T-cell inhibition based on elevation of activation thresholds. Blood. 2001;98:3727–3732. [PubMed: 11739178]

41.

Mishan-Eisenberg G, Borovsky Z, Weber MC. et al. Differential regulation of TH1/TH2 cytokine responses by placental protein 14. J Immunol. 2004;173:5524–5530. [PubMed: 15494501]

42.

Zeiler T, Mäntyjärvi R, Rautiainen J. et al. T cell epitopes of a lipocalin allergen colocalize with the conserved regions of the molecule. J Immunol. 1999;162:1415–1422. [PubMed: 9973397]

43.

Jeal H, Draper A, Harris J. et al. Determination of the T cell epitopes of the lipocalin allergen, Rat n 1. Clin Exp Allergy. 2004;34:1919–1925. [PubMed: 15663569]

44.

Saarelainen S, Zeiler T, Rautiainen J. et al. Lipocalin allergen Bos d 2 is a weak immunogen. Int Immunol. 2002;14:401–409. [PubMed: 11934876]

45.

Kinnunen T, Buhot C, Närvänen A. et al. The immunodominant epitope of lipocalin allergen Bos d 2 is suboptimal for human T cells. Eur J Immunol. 2003;33:1717–1726. [PubMed: 12778490]

46.

Leitenberg D, Bottomly K. Regulation of naive T cell differentiation by varying the potency of TCR signal transduction. Semin Immunol. 1999;11:283–292. [PubMed: 10441214]

47.

Brogdon JL, Leitenberg D, Bottomly K. The potency of TCR signaling differentially regulates NFATc/p activity and early IL-4 transcription in naive CD4+ T cells. J Immunol. 2002;168:3825–3832. [PubMed: 11937535]

48.

Virtanen T, Zeiler T, Mäntyjärvi R. Important animal allergens are lipocalin proteins: Why are they allergenic? Int Arch Allergy Immunol. 1999;120:247–258. [PubMed: 10640908]

49.

Spitzauer S, Pandjaitan B, Mühl S. et al. Major cat and dog allergens share IgE epitopes. J Allergy Clin Immunol. 1997;99:100–106. [PubMed: 9003217]

50.

Cabanas R, Lopez-Serrano MC, Carreira J. et al. Importance of albumin in cross-reactivity among cat, dog and horse allergens. J Investig Allergol Clin Immunol. 2000;10:71–77. [PubMed: 10879993]

51.

Fahlbusch B, Rudeschko O, Schlott B. et al. Further characterization of IgE-binding antigens from guinea pig hair as new members of the lipocalin family. Allergy. 2003;58:629–634. [PubMed: 12823123]

52.

Reddy BM, Karande AA, Adiga PR. A common epitope of β-lactoglobulin and serum retinol-binding proteins: elucidation of its core sequence using synthetic peptides. Mol Immunol. 1992;29:511–516. [PubMed: 1373468]

53.

Marchese S, Pes D, Scaloni A. et al. Lipocalins of boar salivary glands binding odours and pheromones. Eur J Biochem. 1998;252:563–568. [PubMed: 9546674]

54.

Mäntyjärvi R, Parkkinen S, Rytkönen M. et al. Complementary DNA cloning of the predominant allergen of bovine dander: a new member in the lipocalin family. J Allergy Clin Immunol. 1996;97:1297–1303. [PubMed: 8648026]

55.

Rautiainen J, Rytkönen M, Syrjänen K. et al. Tissue localization of bovine dander allergen Bos d 2. J Allergy Clin Immunol. 1998;101:349–353. [PubMed: 9525451]

56.

Rautiainen J, Auriola S, Konttinen A. et al. Two new variants of the lipocalin allergen Bos d 2. J Chromatogr B Biomed Sci Appl. 2001;763:91–98. [PubMed: 11710588]

57.

Rautiainen J, Auriola S, Rouvinen J. et al. Molecular and crystal properties of Bos d 2, an allergenic protein of the lipocalin family. Biochem Biophys Res Commun. 1998;247:746–750. [PubMed: 9647765]

58.

Rouvinen J, Rautiainen J, Virtanen T. et al. Probing the molecular basis of allergy - Three-dimensional structure of the bovine lipocalin allergen Bos d 2. J Biol Chem. 1999;274:2337–2343. [PubMed: 9891000]

59.

Zeiler T, Taivainen A, Rytkönen M. et al. Recombinant allergen fragments as candidate preparations for allergen immunotherapy. J Allergy Clin Immunol. 1997;100:721–727. [PubMed: 9438477]

60.

Kauppinen J, Zeiler T, Rautiainen J. et al. Mutant derivatives of the main respiratory allergen of cow are less allergenic than the intact molecule. Clin Exp Allergy. 1999;29:989–996. [PubMed: 10383601]

61.

de GrootH, Goei KG, van Swieten P. et al. Affinity purification of a major and a minor allergen from dog extract: serologic activity of affinity-purified Can f I and of Can f I-depleted extract. J Allergy Clin Immunol. 1991;87:1056–1065. [PubMed: 2045611]

62.

Ford AW, Kemeny DM. The allergens of dog. II. Identification and partial purification of a major dander allergen. Clin Exp Allergy. 1992;22:793–803. [PubMed: 1525699]

63.

Walls AF, Newman TaylorAJ, Longbottom JL. Allergy to guinea pigs: I. Allergenic activities of extracts derived from the pelt, saliva, urine and other sources. Clin Allergy. 1985;15:241–251. [PubMed: 4006174]

64.

Dandeu JP, Rabillon J, Carmi-Leroy A. et al. The horse major allergen and its close structural relationship to the mouse and rat urinary protein. J Allergy Clin Immunol. 1995;95:348.

65.

Gregoire C, Rosinski-Chupin I, Rabillon J. et al. cDNA cloning and sequencing reveal the major horse allergen Equ c 1 to be a glycoprotein member of the lipocalin superfamily. J Biol Chem. 1996;271:32951–32959. [PubMed: 8955138]

66.

Lascombe M-B, Gregoire C, Poncet P. et al. Crystal structure of the allergen Equ c 1 - A dimeric lipocalin with restricted IgE-reactive epitopes. J Biol Chem. 2000;275:21572–21577. [PubMed: 10787420]

67.

Bulone V, Rademaker GJ, Pergantis S. et al. Characterisation of horse dander allergen glycoproteins using amino acid and glycan structure analyses - A mass spectrometric method for glycan chain analysis of glycoproteins separated by two-dimensional electrophoresis. Int Arch Allergy Immunol. 2000;123:220–227. [PubMed: 11112858]

68.

Goubran BotrosH, Poncet P, Rabillon J. et al. Biochemical characterization and surfactant properties of horse allergens. Eur J Biochem. 2001;268:3126–3136. [PubMed: 11358533]

69.

Lorusso JR, Moffat S, Ohman JLJ. Immunologic and biochemical properties of the major mouse urinary allergen (Mus m I). J Allergy Clin Immunol. 1986;78:928–937. [PubMed: 3097107]

70.

Cavaggioni A, Mucignat-Caretta C. Major urinary proteins, a_2u-globulins and aphrodisin. Biochim Biophys Acta. 2000;1482:218–228. [PubMed: 11058763]

71.

Clark AJ, Clissold PM, Al Shawi R. et al. Structure of mouse major urinary protein genes: different splicing configurations in the 3'-non-coding region. EMBO J. 1984;3:1045–1052. [PMC free article: PMC557469] [PubMed: 6329733]

72.

Clissold PM, Bishop JO. Variation in mouse major urinary protein (MUP) genes and the MUP gene products within and between inbred lines. Gene. 1982;18:211–220. [PubMed: 6290324]

73.

Böcskei Z, Groom CR, Flower DR. et al. Pheromone binding to two rodent urinary proteins revealed by X-ray crystallography. Nature. 1992;360:186–188. [PubMed: 1279439]

74.

Ferrari E, Lodi T, Sorbi RT. et al. Expression of a lipocalin in Pichia pastoris: secretion, purification and binding activity of a recombinant mouse major urinary protein. FEBS Lett. 1997;401:73. [PubMed: 9003809]

75.

Price JA, Longbottom JL. Allergy to rabbits. II. Identification and characterization of a major rabbit allergen. Allergy. 1988;43:39–48. [PubMed: 3344934]

76.

Baker J, Berry A, Boscato LM. et al. Identification of some rabbit allergens as lipocalins. Clin Exp Allergy. 2001;31:303–312. [PubMed: 11251632]

77.

Warner JA, Longbottom JL. Allergy to rabbits. III. Further identification and characterisation of rabbit allergens. Allergy. 1991;46:481–491. [PubMed: 1796773]

78.

Vandoren G, Mertens B, Heyns W. et al. Different forms of a_2u-globulin in male and female rat urine. Eur J Biochem. 1983;134:175–181. [PubMed: 6190651]

79.

Bayard C, Holmquist L, Vesterberg O. Purification and identification of allergenic α2u-globulin species of rat urine. Biochim Biophys Acta. 1996;1290:129–134. [PubMed: 8645715]

80.

Unterman RD, Lynch KR, Nakhasi HL. et al. Cloning and sequence of several α2u-globulin cDNAs. Proc Natl Acad Sci USA. 1981;78:3478–3482. [PMC free article: PMC319592] [PubMed: 6167987]

81.

Larche M. Inhibition of human T-cell responses by allergen peptides. Immunology. 2001;104:377–382. [PMC free article: PMC1783330] [PubMed: 11899422]

82.

Anderton SM. Peptide-based immunotherapy of autoimmunity: a path of puzzles, paradoxes and possibilities. Immunology. 2001;104:367–376. [PMC free article: PMC1783326] [PubMed: 11899421]