No abstract

Cystic fibrosis (CF) is a multisystem autosomal recessive disorder caused by mutations of the cystic fibrosis transmembrane regulator (CFTR), a protein that regulates cyclic-AMP-mediated chloride conductance at the apical membrane of secretory epithelia. Mutations in the CFTR gene are common in many populations. In North America, 4-5% of the general population are heterozygous for a CFTR mutation. Although there are over 400 known CFTR mutations, a single mutation, a deletion of the phenylalanine at position 508 (delta F508) in exon 10, accounts for about 70% of all CF chromosomes worldwide. The reasons for the high frequency of the delta F508 CFTR allele--the selective advantage associated with CF heterozygosity--are unknown. Many physiological abnormalities have been observed in CF heterozygotes, although the clinical significance of these observations is unknown. Preliminary unpublished data and anecdotal information from CF families suggested that, remarkably, the delta F508 allele might protect heterozygotes against bronchial asthma prompted us to further investigate this possibility. Here we present evidence that the delta F508 CF allele protects against asthma in childhood and early adult life.

vaccine administration data are reported to CDC by multiple entities using immunization information systems, the Vaccine Administration Management System, pharmacy systems, or direct submission of electronic health records. (https:// www.cdc.gov/coronavirus/2019-ncov/vaccines/distributing/about-vaccine-data. html). Persons were considered fully vaccinated if they received the second dose in a 2-dose COVID-19 vaccine series (Pfizer-BioNTech or Moderna) or 1 dose of the single-dose Janssen (Johnson and Johnson) COVID-19 vaccine. admissions with confirmed COVID-19 diagnosis (C),** , † † and COVID-19 deaths (D) § §, ¶ ¶ among adults, by age group, and rate ratio for persons aged ≥65 or ≥70 and 18-49 years -United States,