Foreign Body Aspiration Presenting as Pneumothorax in a Child
CUREUS
Authors: Newby, Maxwell D.; Thomas, David; Mullett, Charles J.; Vijay, Chickajajur; Carr, Michele M.
Abstract
A typical presentation of a foreign body aspiration (FBA) in a child includes witnessed choking, respiratory distress, cyanosis, coughing, wheezing, diminished breath sounds, and/or altered mental status. Following an extensive literature review, we found pneumothorax occurring secondary to FBA is a rare occurrence and should elicit prompt treatment. This 17-month-old female was admitted for respiratory syncytial virus (RSV) bronchiolitis and developed a subsequent pneumothorax during her hospital stay, consequent to aspiration of a cashew fragment two weeks before presentation. In light of the National Institute of Allergy and Infectious Diseases (NIAID)-sponsored expert panel's addended guidelines, published and endorsed by the American Academy of Pediatrics (AAP) in 2017, we highlight a potential complication of increasing encouragement of peanut consumption in children as young as four months.
MAVS Deficiency Is Associated With a Reduced T Cell Response Upon Secondary RSV Infection in Mice
FRONTIERS IN IMMUNOLOGY
Authors: Paulsen, Michelle; Varese, Augusto; Pinpathomrat, Nawamin; Kirsebom, Freja C. M.; Paulsen, Malte; Johansson, Cecilia
Abstract
Infections with respiratory syncytial virus (RSV) occurs repeatedly throughout life because sustained, protective memory responses fail to develop. Why this occurs is not known. During RSV infection the recognition of the virusviathe cytosolic RIG-I like receptors and signalingviathe adaptor protein MAVS is crucial for mounting an innate immune response. However, if this signaling pathway is important for T cell responses during primary infection and during re-infection is not fully elucidated. We describe a second peak of pro-inflammatory mediators during the primary immune response to RSV that coincides with the arrival of T cells into the lung. This second peak of cytokines/chemokines is regulated differently than the early peak and is largely independent of signalingviaMAVS. This was concurrent withMavs(-/-)mice mounting a strong T cell response to primary RSV infection, with robust IFN-gamma; and Granzyme B production. However, after RSV re-infection,Mavs(-/-)mice showed fewer CD4(+)and CD8(+)short term memory T cells and their capacity to produce IFN-gamma; and Granzyme B, was decreased. In sum, cytosolic recognition of RSV is important not only for initiating innate anti-viral responses but also for generating or maintaining efficient, short term T cell memory responses.