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1.
Article in English | MEDLINE | ID: mdl-38347823

ABSTRACT

Summary: BLs allergy is considered a major health issue, as BLs are the most frequently involved in drug allergic reactions. Amoxicillin (AX) is the most frequently involved drug in sensitization among all BLs. AX is commercialized alone or combined to clavulanic acid (CLA) in order to increase the antibiotic spectrum. The growing prescriptions of AX-CLA formulations contributed to increase the role of CLA as an allergy inducer. At present, little is known about the clinical characteristics of hypersensitivity reactions to clavulanate. The aim of this study was to assess the difference in the prevalence of cutaneous vs systemic reactions in patients who had a documented history of allergic reactions to amoxicillin-clavulanate and tested positive for clavulanate or penicillin/amoxicillin. Our study suggests that patients who presented only muco-cutaneous reactions were more often sensitized to CLA rather than AX.

3.
Eur Ann Allergy Clin Immunol ; 56(1): 17-25, 2024 Jan.
Article in English | MEDLINE | ID: mdl-36927838

ABSTRACT

Summary: Background. International guidelines suggested skin tests with Polyethylene-glycol (PEG) and polysorbate 80 (PS-80), to investigate a possible hypersensitivity to these excipients either to identify subjects at risk of developing allergic reactions to Covid-19 vaccines, or in patients with suspected IgE mediated hypersensitivity reactions (HR) to the Covid-19 vaccine. The main purpose of this study was to investigate the prevalence of PEG and PS sensitization in patients with a clinical history of HR to drugs containing PEG/PS and in patients with a suspected Covid-19 vaccine immediate HR. Methods. This was a multicenter retrospective study conducted by allergists belonging to 20 Italian medical centers. Skin testing was performed in 531 patients with either a clinical history of suspected hypersensitivity reaction (HR) to drugs containing PEG and/or PS-80 (group 1:362 patient) or a suspected HR to Covid-19 vaccines (group 2: 169 patient), as suggested by the AAIITO/SIAAIC guidelines for the "management of patients at risk of allergic reactions to Covid-19 vaccines" [1]. Results. 10/362 (0.02%) had positive skin test to one or both excipients in group 1, 12/169 (7.1%) in group 2 (p less than 0.01). In group 2 HRs to Covid-19 vaccines were immediate in 10/12 of cases and anaphylaxis occurred in 4/12 of patients. Conclusions. The positivity of skin test with PEG and or PS before vaccination is extremely rare and mostly replaceable by an accurate clinical history. Sensitization to PEG and PS has to be investigated in patients with a previous immediate HR to a Covid-19 vaccine, in particular in patients with anaphylaxis.


Subject(s)
Anaphylaxis , COVID-19 , Hypersensitivity, Immediate , Humans , Polysorbates/adverse effects , Polyethylene Glycols/adverse effects , COVID-19 Vaccines/adverse effects , COVID-19/epidemiology , COVID-19/prevention & control , Excipients/adverse effects , Anaphylaxis/diagnosis , Anaphylaxis/epidemiology , Retrospective Studies , Immunization Programs , Skin Tests , Italy/epidemiology
4.
Article in English | MEDLINE | ID: mdl-36515255

ABSTRACT

Summary: The use of acetylsalicylic acid (ASA) desensitization for patients with coronary artery disease (CAD) is growing, but no data are available on desensitization protocol in patients with ASA sensitivity and CAD during pregnancy. This case report shows that ASA desensitization protocol during pregnancy could be safe and effective in a tertiary centre with a multidisciplinary team.

5.
J Chromatogr B Biomed Sci Appl ; 756(1-2): 11-7, 2001 May 25.
Article in English | MEDLINE | ID: mdl-11419701

ABSTRACT

OBJECTIVE: To evaluate incidence and causes of anaphylactic reactions in the emergency room (E.R.) of a general hospital in Milan during a 2-year period. METHODS: We retrospectively studied the computerized records of patients discharged from an E.R. with a diagnosis of anaphylactic reaction. Anaphylaxis was established on the presence of at least two cutaneous, respiratory, gastrointestinal or cardiovascular system symptoms. RESULTS: During 1997 and 1998, out of 38 685 patients referred to the E.R., 13 had severe anaphylaxis with loss of consciousness (LOC) and 127 had anaphylactic symptoms, without LOC. Of the 13 patients with LOC, a possible cause was identified in 12 (five foods, six drugs, one hair dye). In the other 127 patients anaphylaxis was related to foods in 49 cases (38.5%), drugs in 44 (34.6%), unknown causes in 29 (22.8%), hymenoptera stings in two (1.5%), and other causes in three (2.3%). CONCLUSION: The incidence of anaphylactic reactions was 0.4% and mainly affected females and atopic subjects. Foods, particularly fruits and vegetables, appeared to be the most important cause; other important causes were non steroidal antiinflammatory drugs and beta-lactam antibiotics.


Subject(s)
Anaphylaxis/epidemiology , Emergency Service, Hospital/organization & administration , Adult , Aged , Anaphylaxis/etiology , Anaphylaxis/therapy , Drug Hypersensitivity/complications , Female , Food Hypersensitivity/complications , Hospitals, General , Humans , Incidence , Italy , Male , Middle Aged
6.
J Chromatogr B Biomed Sci Appl ; 756(1-2): 85-93, 2001 May 25.
Article in English | MEDLINE | ID: mdl-11419730

ABSTRACT

BACKGROUND: Allergic reactions induced by ingestion of foods containing sesame seeds are a well recognized cause of severe food-induced anaphylaxis. OBJECTIVE: This study aimed to identify and characterize the clinically most important major allergen of sesame seeds. METHODS: Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and IgE immunoblotting were performed on sera of 10 patients selected for severe and documented allergic reaction after eating food containing sesame. The major allergen was purified by gel filtration and characterized by isoelectric point (pI), glycosylation and amino acid sequencing. RESULTS: All the patients had positive IgE antibodies and skin prick tests (SPTs) to sesame. The major, clinically most important allergen was a protein with molecular mass of about 9000. It was not glycosylated, the amino acid sequence showed it was a 2S albumin with a pI of 7.3; the small and the large subunits, forming the whole protein, showed pI values of 6.5 and 6.0.


Subject(s)
Albumins/analysis , Allergens/analysis , Antigens, Plant/analysis , Magnoliopsida/embryology , Seeds/immunology , 2S Albumins, Plant , Adult , Blotting, Western , Child , Chromatography, Gel , Chromatography, High Pressure Liquid , Electrophoresis, Polyacrylamide Gel , Female , Humans , Immunoglobulin E/analysis , Immunoglobulin E/immunology , Isoelectric Point , Male , Molecular Weight , Skin Tests
7.
J Allergy Clin Immunol ; 105(2 Pt 1): 371-7, 2000 Feb.
Article in English | MEDLINE | ID: mdl-10669861

ABSTRACT

BACKGROUND: Apricots are widely grown in Europe, and allergic reactions are becoming more common, especially oral allergy syndrome. Apricot belongs to the botanical subfamily of Prunoideae, which includes peach, the major allergen of which was identified as a 9-kd protein, a lipid transfer protein (LTP). OBJECTIVE: The aim of the study was to evaluate the IgE reactivity pattern to an apricot extract in subjects with allergic reactions to apricot, as demonstrated by a positive oral challenge response. METHODS: Thirty patients were investigated. All the patients displayed oral allergy syndrome (2 with systemic reactions) to apricot, with positive open food challenge responses, skin prick test responses, and serum-specific IgE antibodies to apricot. The IgE reactivity pattern to apricot extract was identified by using SDS-PAGE and immunoblotting. The major allergen, a 9-kd protein, was then purified by HPLC and characterized by periodic acid-Schiff stain, isoelectric point determination, and N-terminal amino acid sequencing. RESULTS: The sera from all patients allergic to apricot recognized the 9-kd protein, whereas none of the other allergens, with molecular weights from 15 to 80 kd, acted as a major allergen. The 9-kd allergen has an isoelectric point of 8.7 and is not glycosylated. Determination of the N-terminal 34 amino acid sequence showed that it belongs to the LTP family, with a 94% homology with the LTP from peach. IgE blotting of the apricot extract was completely inhibited by the 9-kd purified LTP from peach. CONCLUSIONS: The major allergen of apricot is an LTP, which is highly cross-reactive with the LTP from peach.


Subject(s)
Allergens/immunology , Carrier Proteins/immunology , Carrier Proteins/isolation & purification , Fruit/immunology , Plant Proteins/immunology , Rosales/immunology , Adolescent , Adult , Allergens/isolation & purification , Allergens/metabolism , Amino Acid Sequence , Antigens, Plant , Carrier Proteins/metabolism , Chromatography, High Pressure Liquid , Electrophoresis, Polyacrylamide Gel , Female , Food Hypersensitivity/blood , Food Hypersensitivity/immunology , Fruit/adverse effects , Fruit/chemistry , Glycosylation , Humans , Immunoblotting , Immunoglobulin E/immunology , Immunoglobulin E/metabolism , Isoelectric Focusing , Male , Middle Aged , Molecular Sequence Data , Plant Proteins/isolation & purification , Plant Proteins/metabolism , Rosales/chemistry
8.
J Allergy Clin Immunol ; 104(5): 1099-106, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10550759

ABSTRACT

BACKGROUND: Allergy to apple is commonly associated with birch pollinosis because the two share homologous allergens. However, some patients have apple allergy but no birch pollinosis, suggesting that there are allergens that do not cross-react with birch. OBJECTIVE: The aim of the study was to evaluate the IgE reactivity pattern to an apple extract in subjects with allergic reactions to apple, with and without birch hay fever. METHODS: Forty-three patients with oral allergy syndrome for apple and positive open food challenge, skin prick test, and serum specific IgE antibodies to apple were admitted to the study. Thirty-two had birch pollinosis (documented by specific IgE for birch) and 11 were not allergic to birch. The IgE reactivity pattern to apple extract was identified by SDS-PAGE and immunoblotting. The consistent allergen, a 9-kd protein, was then purified by HPLC and characterized by periodic acid-Schiff staining, isoelectric point, and N-terminal amino acid sequencing. RESULTS: The sera from 28% of patients allergic to apple with birch pollinosis, but from all patients allergic only to apple, recognized the 9-kd protein. This protein has an isoelectric point of 7.5 and is not glycosylated. Determination of its partial amino acid sequence showed that it belongs to the family of lipid transfer proteins, which act as major allergens in Prunoideae fruits. CONCLUSIONS: These results indicate that a lipid transfer protein is an important allergen in patients allergic to apple but not to birch pollen. The prevalent IgE reactivity to this allergen in subjects with no birch pollinosis and the physicochemical characteristics of this protein suggest that sensitization may occur through the oral route.


Subject(s)
Allergens/immunology , Carrier Proteins/immunology , Food Hypersensitivity/immunology , Rosales/immunology , Adolescent , Adult , Amino Acid Sequence , Antigens, Plant , Chromatography, Gel/methods , Chromatography, High Pressure Liquid/methods , Chromatography, Ion Exchange/methods , Electrophoresis, Polyacrylamide Gel/methods , Female , Humans , Immunoblotting , Isoelectric Focusing , Male , Middle Aged , Molecular Sequence Data , Periodic Acid-Schiff Reaction , Plant Proteins , Sodium Dodecyl Sulfate , Staining and Labeling/methods
9.
J Allergy Clin Immunol ; 102(6 Pt 1): 1021-7, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9847444

ABSTRACT

BACKGROUND: Only a few studies have investigated the clinical role of food allergens, especially the relationship between sensitization to a given allergen and occurrence of adverse reactions when eating the relevant food item. OBJECTIVE: This study evaluated the clinical role of the allergens of Brazil nut by comparing the patterns of IgE binding in sera from 11 patients with anaphylaxis after eating Brazil nuts with those from 10 subjects with no symptoms to this food item. Both groups had specific IgE to Brazil nut. METHODS: Allergens in the in-house extract of Brazil nut were identified by SDS-PAGE/immunoblotting, the major allergen was purified by HPLC, and its N-terminal sequence was determined by a protein sequencer. RESULTS: SDS-PAGE/immunoblotting detected a number of allergenic components with molecular weights ranging from 4 to 58 kd. All sera from symptomatic patients recognized a 9-kd allergen corresponding (as established by amino acid sequencing) to a 2S albumin already described as a major allergen of Brazil nut, whereas the other allergens each bound IgE from less than 50% of sera. No sera from asymptomatic subjects showed IgE binding to the 9-kd allergen, but they did recognize components from 25 to 58 kd, which are minor allergens. CONCLUSIONS: These findings indicate that the allergen underlying clinical reactions to Brazil nut is a 2S albumin of 9 kd and that in vitro reactivity to this allergen identifies subjects who react in vivo to ingestion of this food.


Subject(s)
Albumins/immunology , Food Hypersensitivity/immunology , Nuts/immunology , Protein Precursors/immunology , 2S Albumins, Plant , Adolescent , Adult , Albumins/antagonists & inhibitors , Albumins/isolation & purification , Amino Acid Sequence , Antigens, Plant , Binding, Competitive , Child , Child, Preschool , Chromatography, High Pressure Liquid , Female , Humans , Immunoblotting , Isoelectric Focusing , Male , Middle Aged , Molecular Sequence Data , Nuts/adverse effects , Periodic Acid-Schiff Reaction , Protein Precursors/antagonists & inhibitors , Protein Precursors/isolation & purification , Sequence Analysis
11.
J Allergy Clin Immunol ; 101(4 Pt 1): 531-7, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9564807

ABSTRACT

BACKGROUND: Allergic reactions to fruits and vegetables are among the most frequent food allergies in adults. Kiwi fruit (Actinidia chinensis) is commonly involved, causing local mucosal, systemic, or both types of symptoms by an IgE-mediated mechanism. In a previous study on 30 patients allergic to kiwi, we identified a major allergen of 30 kd against which all sera tested clearly reacted. Other allergens were detected at 12, 24, and 28 kd. OBJECTIVE: The aim of this study was to fully characterize the major kiwi fruit allergen of 30 kd. METHODS: Allergens were separated and purified by high-performance liquid chromatography with anion-exchange columns. The purity of the single proteins was checked by sodium dodecylsulfate-polyacrylamide gel electrophoresis, and their allergenicity was checked by immunoblotting with a pool of sera from patients allergic to kiwi. The allergens were characterized by isoelectrofocusing and amino acid sequencing, and periodic acid-Schiff stain was used to detect glycoproteins. RESULTS: Proteins of 30, 28, 24, and 17 kd were purified by high-performance liquid chromatography. IgE binding indicated the 30 kd protein, which showed an isoelectric point of 3.5, as the major allergen of kiwi. Determination of its partial amino acid sequence and comparison with the Swiss Protein Bank showed that this was actinidin, the main protein component of kiwi. The 24 and 28 kd proteins had the same N-terminal sequence, which did not correspond to any known protein. The 17 kd protein had a blocked N-terminal sequence. CONCLUSIONS: These results demonstrate that the major allergen of kiwi fruit, Act c 1, is actinidin, a proteolytic enzyme belonging to the class of thiol-proteases. Two other allergens of 24 and 28 kd appear identical on amino acid sequencing.


Subject(s)
Allergens/analysis , Cysteine Endopeptidases/analysis , Fruit/immunology , Amino Acid Sequence , Chromatography, High Pressure Liquid , Cysteine Endopeptidases/chemistry , Humans , Immunoblotting , Isoelectric Focusing , Molecular Sequence Data , Molecular Weight
12.
Acta Haematol ; 93(1): 5-8, 1995.
Article in English | MEDLINE | ID: mdl-7725851

ABSTRACT

It is well known that L-asparaginase (L-Ase) treatment may cause thrombotic events in patients with acute lymphoblastic leukemia (ALL). The mechanism of this effect is not well understood although a reduction in plasma antithrombin III (AT III) levels is observed. In our study, a group of patients treated with L-Ase received AT III concentrates as adjuvant treatment. This adjuvant treatment reduced the levels of plasma D-dimer and thrombin-antithrombin complex, which are considered as early markers of a hypercoagulability state. These preliminary data suggest that large randomized trials will have to be conducted to improve our understanding of the role of AT III concentrates in ALL therapy.


Subject(s)
Antithrombin III/therapeutic use , Asparaginase/therapeutic use , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Thrombosis/blood , Adolescent , Adult , Aged , Asparaginase/adverse effects , Blood Coagulation Tests , Chemotherapy, Adjuvant , Female , Humans , Male , Middle Aged , Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood , Thrombosis/chemically induced , Thrombosis/prevention & control
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