Effects of Photobiomodulation on the Innate Immune System of Neonates and Infants Diagnosed With Acute Respiratory Sintitial Virus Bronchiolitis - Randomized Controlled Trial
Effects of Photobiomodulation on the Innate Immune System of Neonates and Infants Diagnosed With Acute Respiratory Sintitial Virus Bronchiolitis - Randomized Controlled Trial
The innate immune response of children with acute viral bronchiolitis (AVB) caused by respiratory syncytial virus (RSV) in the acute phase and in the resolution phase, is marked by variations in inflammatory and anti-inflammatory mediators, where in the acute phase there is recruitment and activation of multiple cells of the immune system, with consequent increase in the expression of pro-inflammatory mediators. Evidence indicates that there is a considerable increase in tumor necrosis factor-alpha (TNF) , interleukine 6 (IL6), interleukine 1-beta, interleukine 8 (IL8) interleukine 10 (IL10), exposing to IL6, IL8 and IL-10 positively correlated with AVB severity. There are already reports that the transcutaneous application of photobiomodulation (PBM) reaches the lungs, producing positive responses in respiratory pathologies, both acute and chronic . Thus, PBM caused by the use of low-level laser may be a favorable resource to be used in the area of respiratory physiotherapy, specifically in neonatology and pediatrics, since there are studies in both experimental and human models that prove its action on lung cells, acting to reduce airway edema, reduce neutrophil migration to lung tissue and synthesize pro-inflammatory cytokines TNFalpha, IL6 and IL-10. In addition, it is a portable, practical, quick application, with minimal contraindications and possibly better tolerated by the neonatal and pediatric population.
Acute Viral Bronchiolitis (AVB) is the most common disease of the lower respiratory tract in children, being one of the major causes of hospitalization in children under two years of age, especially in winter. It is characterized by inflammation, edema, and necrosis of cells of the small airways epithelium, with increased mucus secretion and bronchospasm. Among the most common pathogens for the development of AVB are rhinovirus, influenza A and B, parainfluenza, metapneumovirus, adenovirus, however, the most common and responsible for 70% of AVB in children under two years of age is respiratory syncytial virus (RSV). RSV is highly contagious and infectious, accounting for 2-3% of the hospitalization of infected children, and there is a seasonal variation in RSV infection levels, which are higher during the winter in temperate regions, and this occurs because low temperatures and high humidity favor the proliferation of the virus.
RSV is transmitted through the air in contact with the nasal epithelium, mouth, eyes, or contaminated surfaces, and the incubation time is three to eight days. As soon as the virus reaches the nose or mouth, it begins to infect the epithelial cells of the upper respiratory tract, then progresses to the lower airways reaching the bronchioles where it replicates more easily, thus developing bronchiolitis. Inflammation and obstruction of the bronchioles then occurs, resulting in reduced airflow in the small caliber airways, altering the ability to exhale, which leads to hyperinflation, increased mucus production, atelectasis and wheezing. Immunopathology occurs through the expression of pro-inflammatory cytokines with subsequent perivascular and peribronchial infiltration of mononuclear cells, mostly neutrophils and lymphocytes, triggering an unbalanced response between T helper cells 1 and 2.
In addition to AVB, RSV infection can lead to pneumonia in addition to the possibility of later development of wheezing and asthma, so there is growing concern about how RSV infections in the first months of life can lead to the development of chronic lung diseases. in addition to being considered the second pathogenic agent causing death in children under one year of age.
The inability of the innate immune system of neonates and children to fight RSV infection and its serious consequences makes the development of new prevention and treatment strategies a priority.
To meet this need, notable advances have been made in recent years in relation to low-level laser PBM applied to lung diseases. PBM is a non-invasive, adverse-effect-free, accessible, and well-tolerated resource for patients diagnosed with pulmonary diseases such as chronic obstructive pulmonary disease, COVID-19 and asthma. Many effects are attributed to PBM and one of the main ones is its antioxidant and anti-inflammatory effects at the cellular level. From the penetration of the photon into the tissue where it interacts with intracellular molecules and initiates a series of changes in its functioning, including membrane permeability and cellular metabolism, regulating antioxidative defenses and reducing oxidative stress.
Jahani-Sherafat et al. (2020) in their review explain the various hypotheses for PBM in cellular functions, the first refers to cytochrome-c oxidase, obtained by infrared light. Other hypotheses are that photons separate nitric oxide from the enzyme and make this nitric oxide active and increase electron transport, mitochondrial membrane potential, and adenosine triphosphate (ATP) production. Another hypothesis is related to light-sensitive ion channels that can lead to the accumulation of calcium in cells, and after photon absorption, several signaling channels are activated using reactive oxygen species, cyclic adenosine monophosphate (AMP), nitric oxide, and calcium, leading to the stimulation of transcription factors. With these factors activated, the expression gene increases and as a result, increases protein synthesis and proliferation, anti-inflammatory signaling, anti-apoptotic proteins, and antioxidant enzymes.
Scientific studies, both in animal and human models, has been developed focused on reducing inflammatory conditions resulting from both acute and chronic respiratory pathologies. In general, these studies demonstrate that the transcutaneous application of PBM reaches the lungs and positively interferes with inflammatory and immunological processes in lung lesions. It can be a viable resource as an adjuvant in the treatment of respiratory pathologies.
Study Design:
The study will be a randomized clinical trial and the sample consisted of neonates and infants from zero to 24 months of age, diagnosed with AVB hospitalized at the Maternal and Child University Hospital of the Universidade Estadual de Ponta Grossa. The project will be submitted for approval by the Human Research Ethics Committee, and subsequently registered in the ClinicalTrials.gov database.
The parents or guardians of the newborn or infant will be invited to participate in the study and, if they are interested, they must consent to participate by signing the free and informed consent form. The purpose of the study will be explained to those responsible and they will be able to ask questions at any time about the procedures to be performed. If the parents or guardians wish to leave the study, there will be no harm to the patient's treatment, which will be as established in the randomization.
The admission of patients diagnosed with AVB to the participating hospitals will be checked daily. As soon as the patient is identified, in the first physical therapy consultation, the person in charge will be invited to participate in the research through the informed consent form. If accepted, the physiotherapist will proceed with the questions on the follow-up form, after which the physiotherapy will follow the physiotherapy service according to the indicated randomization. In this first consultation, the International Study of Wheezing (EISL) questionnaire will be applied, AVB severity will be determined by the Wang scale, and tracheal secretion samples will be collected. The results of routine laboratory tests will be monitored daily to record the values. A new sample of tracheal secretion will be collected on the fourth day of hospitalization, the last sample will be collected on the eighth day of hospitalization or earlier if the patient is discharged from the hospital. For follow-up, the researcher will contact the parents or guardians after completing three months of hospital discharge to apply a questionnaire prepared by the author that will contain the following questions: How many times has your child had a cold/flu in the last few months?; If so, did he/she needed to be hospitalized?; Are your child's vaccinations up to date?; Did your child start attending daycare or school during this period?; Has there been a change in the child's diet? (e.g. food transition); Do you notice your child tired to play?
Randomization and blinding:
Randomization will be done in blocks and generated by a computer program, being concealed in sealed and sequentially numbered opaque envelopes, implemented by someone who has no involvement in the study. Each envelope will correspond to one of the two study groups and an envelope will be chosen by the participant's guardian at the time of evaluation. The statistical evaluator will be blinded to the allocation of patients into the groups.
Due to its originality, this study has great potential for publication in renowned scientific journals. If the hypothesis that MBF promotes the reduction of cellular inflammatory status is confirmed, the benefits will be related to a shorter hospital stay, faster resolution of the lung infection, in addition to consolidating MBF as another effective resource in the respiratory physiotherapy action in the treatment of AVB in this population.
Inclusion Criteria:
Exclusion Criteria:
Diagnosis of congenital or acquired heart disease;
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