Publications by authors named "Mohammad R Fazlollahi"

Background: According to the WHO's recommendation for developing countries, Bacillus Calmette-Guerin (BCG) vaccination has been implemented in some countries as part of national vaccination programs at birth. Although it is generally considered safe, some complications may occur; including BCGitis (local) or BCGosis (systemic), ranging from mild like local abscesses to fatal impediments like osteomyelitis and disseminated BCG infection. This study aimed to determine the spectrum of inborn errors of immunity (IEI) in BCG-vaccinated neonates experiencing local or systemic complications.

View Article and Find Full Text PDF

The purpose of this study is to investigate the effect of air pollutants and noise on the prevalence of childhood asthma in Tehran, Iran. The standardized questionnaire was completed by one of the parents of children aged 6-7 years or by adolescents aged 13-14 years. The asthma prevalence in ages 6-7 and 13-14 was found to be 8.

View Article and Find Full Text PDF
Article Synopsis
  • Primary immunodeficiency diseases with partial albinism, such as Chediak Higashi Syndrome (CHS) and Griscelli Syndrome type 2 (GS2), are autosomal recessive disorders characterized by immune deficiencies and abnormal pigmentation.
  • The study evaluated 25 patients over the past decade, using genetic analyses and examinations of leukocyte granules and hair shafts to identify these conditions, along with control groups of patients with albinism and healthy individuals.
  • The findings indicated specific genetic variants associated with CHS and HPS2, highlighting the importance of timely hematopoietic stem cell transplantation and genetic testing for accurate diagnosis and management of these syndromes.
View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to compare the efficacy, safety, and immunogenicity of a new treatment (P043) for allergic asthma with the established drug, Xolair (omalizumab), focusing on the rate of asthma exacerbations.
  • Over a 28-week trial with 256 participants, results showed that both treatments had similar rates of exacerbations, asthma control test scores, and spirometry measurements, indicating that P043 is as effective as omalizumab.
  • Adverse events reported were comparable between both groups, with common issues being dyspnea and headache, and no significant issues with drug safety or immunogenicity observed for either treatment.
View Article and Find Full Text PDF
Article Synopsis
  • The static charge on plastic spacers for inhaling medications can attract drug aerosols, which decreases the amount of medication available for inhalation.
  • This study tested whether "priming" spacers with 20 puffs of salbutamol could improve lung function in children with mild to moderate asthma.
  • Results showed no significant difference in lung function (measured by FEV1) between using primed and new spacers, indicating that the priming method is not effective in enhancing bronchodilation in clinical settings.
View Article and Find Full Text PDF

Two Iranian patients with purine nucleoside phosphorylase (PNP) deficiency are described in terms of their clinical and molecular evaluations. PNP deficiency is a rare form of combined immunodeficiency with a profound cellular defect. Patients with PNP deficiency suffer from variable recurrent infections, hypouricemia, and neurological manifestations.

View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to establish reference ranges for T cell proliferation induced by phytohemagglutinin (PHA-SI) and Bacillus Calmette-Guérin (BCG-SI) to assist in clinical diagnosis.
  • Researchers evaluated data from 359 healthy children and 35 patients with cellular immunodeficiency using a colorimetric method to measure cell proliferation and determined reference ranges at the 2.5th and 97.5th percentiles.
  • The results showed significant differences in proliferation between healthy controls and patients with immunodeficiency, providing crucial thresholds for diagnosing congenital immunodeficiency diseases.
View Article and Find Full Text PDF

Background: Few studies have evaluated COVID-19 vaccine efficacy in patients with inborn errors of immunity (IEI).

Objective: To evaluate the levels of antibody (Ab) production and function after COVID-19 vaccination in IEI patients with phagocytic, complement, and Ab deficiencies and their comparison with healthy controls.

Methods: Serum samples were collected from 41 patients and 32 healthy controls at least one month after the second dose of vaccination, while clinical evaluations continued until the end of the third dose.

View Article and Find Full Text PDF
Article Synopsis
  • - Severe combined immunodeficiency (SCID) is a serious genetic disorder affecting the immune system, leading to critical infections, with variances in disease presentation complicating timely diagnosis.
  • - A study described four patients, including both typical and atypical SCID cases, who showed symptoms within six months of birth with various genetic mutations identified, such as in the RAG2, IL7R, ADA, JAK3, LIG4, and LAT genes.
  • - The findings provide insights into the genetic diversity of SCID and emphasize the importance of early diagnosis and management for affected individuals, including the confirmation of mutations through Sanger sequencing in both patients and their parents.
View Article and Find Full Text PDF
Article Synopsis
  • This study analyzed 69 patients suspected of having Leukocyte Adhesion Deficiency-I (LAD-I) over a 15-year period to better classify the severity based on clinical, laboratory, and genetic findings.
  • The majority of patients were diagnosed at a median age of 6 months, with a notable delayed diagnosis and high rates of severe cases, leading to a 44.9% mortality rate.
  • Genetic testing revealed several mutations associated with the disease, highlighting the importance of early detection and awareness among physicians to improve patient outcomes and support families with a history of LAD-I.
View Article and Find Full Text PDF

Aim: Increased IgE levels have made house dust mite allergens one of the most frequent causes of allergies worldwide. Treatment reduces the IgE antibodies and types two cytokines, namely interleukin-4 (IL-4) and IL-13. Although existing treatments significantly reduce IgE or IL-4/IL-13, they are very costly.

View Article and Find Full Text PDF
Article Synopsis
  • - Griscelli syndrome type 2 (GS2) is a rare genetic disorder caused by mutations in the RAB27A gene, leading to symptoms like hair color changes, recurrent infections, and blood issues in affected individuals.
  • - This study focused on 18 Iranian children with GS2, uncovering novel mutations in the RAB27A gene through genetic testing techniques like PCR and whole-exome sequencing.
  • - The research identified a common mutation (c.514_518delCAAGC) found in 10 of the patients, suggesting it may be prevalent in Iran; early diagnosis is essential to improve treatment outcomes, including potential stem cell transplantation.
View Article and Find Full Text PDF

Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder more common in autosomal recessive (AR) than X-linked in Iran. This study aimed to assess whether having a child with AR-CGD would increase the likelihood of the next child being affected by CGD. Ninety-one families with at least one child affected by AR-CGD entered this study.

View Article and Find Full Text PDF

Allergen-specific immunotherapy (AIT) involves administering allergen extracts. It is used to desensitize allergic patients. Herbal allergen extracts that are optimum in efficacy and fewest in side effects are still challenging to produce.

View Article and Find Full Text PDF

Early diagnosis of primary immunodeficiencies is crucial for timely treatment and preventing unwanted complications. Next-generation sequencing (NGS) and detailed clinical and immunological evaluation can help early detect such disorders. This study aimed to confirm the diagnosis of two cases of autosomal recessive hyper-immunoglobulin E (IgE) syndrome (AR-HIES), presenting with irreversible eye involvement.

View Article and Find Full Text PDF
Article Synopsis
  • - Recent advancements in molecular diagnosis of allergies have led to the development of the friendly allergen nano-bead array (FABER), a multiplex assay that tests for specific IgE against 244 different allergens in a routine manner.
  • - A study involving 60 allergic patients assessed their IgE sensitization patterns using the FABER test, which identifies responses to both inhalant and food allergens.
  • - Results indicated that common allergenic sensitizations included certain grasses and their components, with findings showing higher rates of sensitization to specific grass proteins compared to previous extract-based tests.
View Article and Find Full Text PDF
Article Synopsis
  • - Chronic granulomatous disease (CGD) is a serious immune disorder treated primarily through hematopoietic stem cell transplantation (HSCT), which was studied in 15 patients using a combination of specific drugs for better outcomes.
  • - The study showed a three-year overall survival rate of 73.3% and an event-free survival rate of 46.7%, with about 73% of patients achieving full donor chimerism.
  • - The results suggest that HSCT with these treatments is effective for CGD, with recommendations to proceed quickly once a matched donor is identified; however, there is a notable risk of transplant-related mortality, especially in adults.
View Article and Find Full Text PDF

Noise has been reported as one of the most important risk factors for asthma, but there are some disagreements. This study aimed to investigate the effect of road noise on asthma prevalence in adults. In the current study, 3172 adults were interviewed through the ECRHS standardized questionnaire in Tehran, the capital of Iran.

View Article and Find Full Text PDF

T-cell receptor excision circles (TREC)/Kappa-deleting recombination excision circles (KREC) assay has been recently recognized for detecting patients with primary (T- and/or B-cell) immunodeficiency (PID). We aimed to investigate the alterations of these biomarkers in some combined immunodeficiency patients compared to the healthy controls in different age groups. TREC and KREC were assessed in a total of 82 PID patients, most of them with exact genetic diagnosis (3 months to 42 years); using quantitative real-time-polymerase chain reaction (PCR).

View Article and Find Full Text PDF

Purpose: This study aimed to determine the impact of MI on self-efficacy, beliefs about medicines and medication adherence among adolescents with asthma.

Method: This randomized controlled trial conducted on 52 adolescents with asthma referring to the Pediatric Medical Center in Tehran, Iran. They were randomly assigned to the control and intervention groups.

View Article and Find Full Text PDF

Exosomes are extracellular vesicles that are involved in intracellular communication and different biological processes. Recently, the importance of microRNAs (miRNAs) in exosomes has been considered as biomarkers in asthma diagnosis. This study aimed to determine the expression of selective miRNAs from plasma-derived exosomes in moderate and severe asthmatic patients compared with healthy controls.

View Article and Find Full Text PDF

This study aims to investigate the role of prenatal diagnosis (PND) in Iranian couples with a previous history of primary immunodeficiency disorders (PIDD) in their family. All referred couples with a family history of PIDD and a tendency for PND were included in this project. Based on gestational age, chorionic villus sampling (CVS) was performed to analyze the molecular defect of the fetus according to the previous gene defect of the affected case in the family.

View Article and Find Full Text PDF

The skin prick test (SPT) could be applied as a useful in vivo method for the detection of sensitization in epidemiological and diagnostic studies if the wheal size is ideally evaluated. We focused on SPT wheal size to identify sensitization pattern to common inhalant and food allergens. In this cross-sectional study, SPT results were obtained from a total of 972 allergic patients.

View Article and Find Full Text PDF
Article Synopsis
  • Hereditary Angioedema (HAE) is a rare genetic disorder caused by mutations in the C1 inhibitor gene, leading to two types: type I (genetic deficiency) and type II (functional deficiency).
  • A study involving 34 Iranian patients found that 23 had HAE type I and 11 had HAE type II, identifying 14 unique pathogenic mutations, including novel ones that had not been previously reported.
  • The research highlights the importance of genetic testing in diagnosing HAE, which can help prevent severe complications and improve early detection, especially in children and asymptomatic individuals.
View Article and Find Full Text PDF