Antibody Isotype and Subclass Responses in Human Patients With Different Clinical Presentations of Sporotrichosis

• Published in: Mycoses 2024-09, Vol.67 (9), p.e13793-n/a
• Main Authors: Almeida‐Paes, Rodrigo, Lugones, Camila Jantoro Guzman, Almeida, Marcos Abreu, Quintana, Marcel de Souza Borges, Benevides‐Freitas, Maurício Sá, Ribeiro, Joyce Rodrigues, Freitas, Dayvison Francis Saraiva, Macedo, Priscila Marques, Valle, Antonio Carlos Francesconi, Zancopé‐Oliveira, Rosely Maria, Gutierrez‐Galhardo, Maria Clara
• Format: Article
• Language: English
• Subjects: Adult; Aged; Antibodies; Antibodies, Fungal - blood; Antigens, Fungal - blood; Antigens, Fungal - immunology; diagnosis; ELISA; Enzyme-Linked Immunosorbent Assay; Female; Humans; humoral immune response; Hypersensitivity; Immunoglobulin A; Immunoglobulin A - blood; Immunoglobulin G; Immunoglobulin G - blood; Immunoglobulin Isotypes - blood; Immunoglobulin Isotypes - immunology; Immunoglobulin M; Immunoglobulin M - blood; Isotypes; Male; Middle Aged; Patients; Sensitivity analysis; Sensitivity and Specificity; Sporothrix; Sporothrix - classification; Sporothrix - immunology; Sporotrichosis; Sporotrichosis - diagnosis; Sporotrichosis - immunology; Young Adult
• ISSN: 0933-7407; 1439-0507; 1439-0507
• DOI: 10.1111/myc.13793

ABSTRACT Sporotrichosis diagnosis involves a series of analyses, including culture and antibody detection in serum samples. Serologic methods may sometimes yield false‐negative or false‐positive results, leading to inaccurate diagnoses. This study assessed specific patient groups in which antibody detection of different isotypes and subclasses may lack sensitivity. An enzyme‐linked immunosorbent assay (ELISA) with Sporothrix brasiliensis exoantigens was used to investigate IgM, IgG, IgG1, IgG2, IgG3, IgG4, IgA, IgA1 and IgA2 antibodies in human serum samples. Eighty serum samples from patients with different sporotrichosis clinical manifestations, including cutaneous forms with and without hypersensitivity manifestations, extracutaneous forms (bone, ocular, meningeal and pulmonary), disseminated cutaneous forms and disseminated forms in individuals living with HIV/AIDS, diabetics and alcoholics, were evaluated. The ELISA sensitivities in the detection of different antibodies ranged from 0.85 to 0.60 for the detection of IgG2 and IgG3, respectively. The antibodies with higher area under ROC curves were IgG2, IgG, IgA and IgA1. There were no significant differences in the immunological reactivity of the tested antibodies among different clinical forms of sporotrichosis. The data revealed a higher likelihood of a false‐negative outcome in patients with lesions in the nasal mucosa regarding the detection of IgM and a lower likelihood in patients with lymphocutaneous sporotrichosis regarding the detection of IgG3. Patients with hypersensitivity manifestations had a 3.71 odds ratio to yield negative results in total IgG detection. In conclusion, we identified specific patient groups in which antibody detection may lack sensitivity, thus contributing to a better understanding of the diagnostic challenges associated with this condition.