key: cord-0906328-vl86o8sf authors: Santos, Júlia Gaspar de Oliveira; Migueis, Débora Petrungaro; Amaral, Jônatas Bussador do; Bachi, André Luis Lacerda; Boggi, Alexandre Coelho; Thamboo, Andrew; Voegels, Richard Louis; Pezato, Rogério title: Impact of SARS-CoV-2 on saliva: TNF-⍺, IL-6, IL-10, lactoferrin, lysozyme, IgG, IgA, and IgM date: 2022-01-25 journal: J Oral Biosci DOI: 10.1016/j.job.2022.01.007 sha: afce8f076d94123c1493215c664ef603b3c14b3d doc_id: 906328 cord_uid: vl86o8sf OBJECTIVES: Understanding the role of certain salivary components, such as TNF-⍺, IL-6, IL-10, lactoferrin, lysozyme, IgG, IgA, and IgM, in airway defense during the ongoing SARS-CoV-2 pandemic is essential. The salivary immune barrier of patients with COVID-19 may play a role in their prognosis. The present study aims to evaluate the impact of SARS-CoV-2 on saliva composition. METHODS: A longitudinal study was carried out with male and female firefighters aged 24–48 years. The study sample (n = 34) was divided into 3 groups: asymptomatic volunteers with a negative polymerase chain reaction (PCR) test for SARS-CoV-2 (group 1, Control, n = 21); patients with symptoms of COVID-19 of less than 7 days’ duration and a diagnosis of SARS-CoV-2 infection by PCR (group 2, COVID-19, n = 13); and recovered patients from group 2 who were free of COVID-19 symptoms for at least 2 months (group 3, post-COVID-19 recovery, n = 13). All groups underwent real-time PCR to detect the presence of SARS-CoV-2, as well as analysis of the salivary concentrations of TNF-⍺, IL-6, IL-10, lactoferrin, lysozyme, IgG, IgA, and IgM by the ELISA method. RESULTS: Lactoferrin concentrations were significantly decreased in the infected group (COVID-19) when compared to those not infected by SARS-CoV-2 (control) (p = 0.032). IgA concentrations were decreased in the COVID-19 and post-COVID-19 groups compared to the control group (p = 0.005 and p = 0.016, respectively). Comparison of the COVID-19 and post-COVID-19 groups also revealed an increase in IgM concentrations during acute SARS-CoV-2 infection (p = 0.010). CONCLUSION: SARS-CoV-2 alters the composition of the salivary immune barrier. In December 2019, a cluster of pneumonia cases of unknown etiology emerged in Wuhan, China [1] . As the disease continued to spread rapidly, an epidemiological and etiological investigation detected a novel type of coronavirus [2] . This infection was named coronavirus disease 2019 (COVID-19) by the World Health Organization (WHO) [3] . In a short time, the virus spread globally and was declared a public health emergency of international concern by WHO [4] . Coronaviruses (CoVs) are enveloped, single-stranded RNA viruses belonging to the Coronaviridae family [5] . Person-to-person spread occurs through close contact, either with patients or with asymptomatic carriers [6] . Close contact or shortrange transmission of infectious saliva droplets is the primary mode of SARS-CoV-2 spread, while long-range transmission of saliva via aerosols is highly dependent on the environment, occurring mostly in aerosol-generating indoor settings [7] . Once in the body, the coronavirus enters host cells by binding via its spike glycoprotein to the angiotensin-converting enzyme II (ACE2) receptor [5, 8] . After fusion, viral RNA is released into the cytoplasm and forms a complex for replication and transcription, which will produce proteins for the assembly of new virions [6] . COVID-19 has an incubation period of approximately 4 to 6 days [9] . It affects mostly males (55.6%), with a mean age of 46.62 years [10] , although the age range is COVID-19=Coronavirus Disease 2019 WHO=World Health Organization CoVs=Coronaviruses ACE2=Angiotensin-Converting Enzyme II IFN=Interferon IL=Interleukins Lf=Lactoferrin TNF-⍺= Tumor Necrosis Factor-alpha J o u r n a l P r e -p r o o f quite broad [11, 12] . The clinical manifestations of COVID-19 are protean, varying widely in terms of both symptoms and severity. Signs and symptoms include fever, conjunctival injection, headache, cough, hemoptysis, fatigue, nausea, vomiting, diarrhea, arthralgia, dyspnea, anorexia, myalgia, abdominal pain, and weakness [4, 13] . Fever, cough, and dyspnea are the most common manifestations [14] . The innate immune response is the first to be triggered in the presence of the virus, inducing the expression of inflammatory factors, dendritic cell maturation, and interferon (IFN) synthesis; this speeds virus phagocytosis by macrophages, thus slowing its spread [15] . However, previous studies of SARS-CoV-2 have shown that its N protein is capable of interfering with the RNA recognition step of the innate immune response, thus suppressing IFN synthesis [16] . The adaptive immune response begins with the activation of CD4 and CD8 T lymphocytes, which aim to stimulate the production of antibodies by B cells and proinflammatory cytokines by T cells, respectively. Another mechanism of CoV pathogenesis is the inhibition of T-cell functions, culminating in their apoptosis [5] . During the disease course, there is an increase in levels of cytokines such as interleukins (IL) (IL-1, IL-2, IL-4, IL-7, IL-10, IL12, IL-13, IL-17) , granulocytemacrophage colony-stimulating factor (GM-CSF), IFN gamma, and tumor necrosis factor; this is one of the major mechanisms implicated in clinical deterioration [6, 17] . Saliva is a fluid secreted by salivary glands in the oral cavity. It is composed of water, electrolytes, and proteins, among other constituents. Among the component proteins of saliva, lactoferrin, lysozyme, cytokines, and immunoglobulins are key, as they act as a first line of immune defense against the entry of harmful agents [18] . Lactoferrin (Lf) is a naturally occurring, multifunctional globular glycoprotein present in saliva, tears, sperm, and colostrum, with the highest available concentrations in the latter. In vitro, Lf has shown antiviral efficacy against a wide J o u r n a l P r e -p r o o f range of viruses, including SARS-CoV-2. In addition, it has unique immunomodulatory and anti-inflammatory effects that may be especially relevant to the pathophysiology of severe cases of COVID-19 [19] . Lysozyme, in turn, is an enzyme capable of hydrolyzing bacterial cell wall bonds. It can be found in tears, mucus, breast milk, and saliva. By its mechanism of action, it contributes to the immune response against infections [20] . Cytokines are glycoproteins capable of modulating the host inflammatory response. Interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-⍺) are two of the main pro-inflammatory cytokines. IL-6 is released by macrophages and T cells, playing an important role in fever induction and in the response to acute inflammation, stimulating the production of other cytokines and B cell growth. TNF-⍺ is produced by macrophages, lymphocytes, and monocytes, and its release recruits neutrophils and monocytes to the site of inflammation [21] . Conversely, interleukin 10 (IL-10) is a major immunosuppressant and antipyretic agent. It is a macrophage deactivating factor and has neutrophil-inhibiting effects. In fact, some infectious agents induce IL-10 synthesis or encode their own IL-10 homologs, resulting in suppression of the host immune response [22] . There are five different classes of immunoglobulins (IgM, IgG, IgE, IgA, and IgD). IgA protects against infections of the mucous membranes that line the mouth, airways, and gastrointestinal tract. It is also found in saliva, tears, and breast milk. IgM is the first immunoglobulin to appear in the immune response, clearing pathogens in their earliest stages. IgG is the main type of antibody (accounting for three-quarters of total blood immunoglobulin), especially in secondary responses, and its levels can be elevated in several conditions, including autoimmune diseases and infections. It is capable of entering tissues to fight infection [23] . Understanding the role of certain salivary components in airway defense is essential in a pandemic such as COVID-19. Furthermore, saliva itself offers an J o u r n a l P r e -p r o o f ecological niche for colonization by oral microorganisms, which can prevent the overgrowth of other, more aggressive pathogens. It is also useful as a noninvasive diagnostic tool for virus detection and surveillance of immune status. On the other hand, it is also the main substrate for viral transmission, through droplets and aerosols [24] . In COVID-19, respiratory failure is the dominant condition in more severe cases, whether due to diffuse alveolar damage caused by inflammation or to direct infection of the lung tissues. Since secondary pulmonary infections can be partially facilitated or hindered by changes in the innate and adaptive barriers of the upper airways, such as saliva, research into the effects of SARS-CoV-2 on the oral mucosa is essential to understand whether this virus modifies this immune barrier and, if so, how and to which extent this influences its penetration into the host [25] . This longitudinal study was carried out on a sample of firefighters from the city of São Paulo, of both sexes, aged between 24 and 48 years. The project was approved by the Research Ethics Committee and registered on Plataforma Brasil (CAAE: 39223320.9.1.1001.5505). The inclusion criteria were age between 18 and 65 years and having passed the annual fire department physical evaluation. The exclusion criteria were: unwillingness to participate in the study; chronic or acute sinusitis; history of chronic diseases of the oral cavity, pharynx, or larynx; systemic or autoimmune diseases; and chronic intake of corticosteroids and/or anti-inflammatory drugs up to one month before specimen collection. The sample comprised 34 volunteers. For research purposes, it was divided into 3 groups: asymptomatic volunteers with a negative PCR test for SARS-CoV-2 (group 1, Control, n=21); patients with symptoms of COVID-19 of less than 7 days' duration, no indications for hospital admission, and a diagnosis of SARS-CoV-2 infection by PCR (group 2, COVID-19, n=13); and participants from group 2 once they had been free of COVID-19 symptoms for at least 2 months (group 3, recovery, n=13). In all groups, concentrations of TNF-⍺, IL-6, IL-10, lactoferrin, lysozyme, IgG, IgA, and IgM in saliva were analyzed. Participants' saliva was stored at -80 °C at an Otorhinolaryngology Research Laboratory where TNF-⍺, IL-6, IL-10, lactoferrin, lysozyme, IgG, IgA, and IgM measurements were also performed. Cytokines (IL-6, IL-10, and TNF-α) were quantitated using commercial ELISA assays (Thermo Fisher Scientific, Invitrogen, Vienna, Austria; catalog numbers 88-7066, 88-7106, and 88-7346 respectively), following the manufacturer's instructions, and results expressed as pg/mL. The antimicrobial peptides (lactoferrin and lysozyme) were also measured by ELISA (EZ Assays, Florida, USA). Results were expressed as µg/mL for lactoferrin and ng/mL for lysozyme (catalog numbers Ck-bio-12222 and Ck-bio-12360, respectively). Concentrations of anti-SARS-CoV-2 IgA, IgM, and IgG were also determined by ELISA in the saliva specimens. Reaction plates were coated with optimal concentrations of SARS-CoV-2 N, M, and S antigens. After blocking of non-specific binding sites, saliva specimens were diluted in PBS-Tween 0.1% buffer containing 1M NaCl, at a 1:2,000 ratio for IgA and IgM and 1:5,000 for IgG, added to the J o u r n a l P r e -p r o o f previously coated and blocked plate, and left to incubate for at least 2 hours at 37 °C. After incubation and washing of each well of the plate, human anti-IgA (1:2,000), anti-IgM (1:2,000), and anti-IgG (1:10,000) conjugate were added and the plate kept for at least 1 hour at 37ºC. The reaction was assessed by adding TMB solution to each well of the plate, followed by a stop buffer (4N H2SO4) to interrupt the reaction. The reaction was then read at 450 nm in a microplate reader (Labsystem Mulitskan MS). The measured concentrations of antimicrobial peptides (lactoferrin and lysozyme), cytokines (IL-6, IL-10, TNF-⍺), and immunoglobulins (IgA, IgM, and IgG) in saliva were then compared between groups to assess the impact of SARS-CoV-2. Data were analyzed in Jamovi version 1.8.4. Quantitative variables were described as mean (standard deviation) or median (interquartile range) as appropriate. The Shapiro-Wilk test was used to test the assumption of normality for quantitative variables. Between-group homogeneity of age and sex distribution was evaluated using Student's t-test for independent samples and Fisher's exact test, respectively. The nonparametric Wilcoxon test was used to compare the expression of the markers of interest between the COVID-19 and post-COVID-19 groups. Comparisons among the COVID-19, post-COVID-19, and Control groups were performed using Student's t-test or the nonparametric Mann-Whitney test. P-values <0.05 were considered statistically significant. First, groups were examined for homogeneity regarding age and sex. Table 1 below presents descriptive statistics for these two variables across groups, with the J o u r n a l P r e -p r o o f respective p-values. The results indicate that there is a significant difference in participant age between the groups (p=0.019). On average, participants in the COVID-19 group were 5.3 years older than those in the control group. No significant difference was found regarding sex distribution (p=1). Although there is a statistical difference in age between the control group and the infected group, this difference was not clinically important, as the mean age ranged from 34 to 39 years between groups. Regarding sex, studies have reported an alternating predominance among those infected with SARS-CoV-2 [13, 26] . In our study, as our sample was composed of firefighters and firefighting is a predominantly male occupation, a higher prevalence of male patients was expected. No significant difference in sex distribution was found between the control and COVID-19 groups. The pro-inflammatory cytokines IL-6 and TNF were not significantly altered in J o u r n a l P r e -p r o o f patients with COVID-19, suggesting that there was no intense inflammatory response in the saliva. However, a decrease in concentrations of IL-10 was observed in the post-COVID-19 group when compared to the control. This cytokine promotes immune regulation, inactivating macrophages and limiting the inflammatory response. A prior study, however, found that one of the features of the immune response in COVID-19 is marked elevation of serum concentrations of IL-10, especially in patients with a severe and critical illness. Although the exact mechanism of this response remains unknown, meta-analyses have found that high levels of IL-10 could be used as predictors of disease severity. In short, this cytokine is believed to play a prognostic role in the pathophysiology of SARS-CoV-2 infection [22] . In blood samples from 102 hospitalized patients with COVID-19, categorized into moderate, severe, and critical conditions, high serum concentrations of TNF-⍺, IFN-gamma, IL-2, IL-4, IL-6, and IL-10 were found in comparison to a control group. The same study also found that measurement of IL-6 and IL-10 could be used as a rapid means of identifying patients at higher risk of progressing to severe disease [18] . Research has reported elevation of IL-1, IL-2, IL-4, IL-7, IL-10, IL12, IL-13, IL-17, GM-CSF, IFN-gamma, TNF during the disease course of COVID-19, and suggested that this is one of the major mechanisms implicated in clinical deterioration [6, 17] . Many studies have measured cytokine levels in the peripheral blood of critically ill patients during the acute phase of illness, unlike this study, in which salivary cytokine levels were evaluated in patients with mild COVID-19. In contrast, Merza et al. compared cytokine levels in the blood of patients with moderate COVID-19, severe COVID-19, and recovered from COVID-19, and found IL-10 concentrations to be significantly higher in the group of recovered patients compared to those with active disease; this may corroborate its role in regulating inflammation [27] . In the present study, there was no significant difference in IL-6 concentrations between the control and COVID-19 groups. However, in other studies which J o u r n a l P r e -p r o o f evaluated serum levels of inflammatory markers, IL-6 values were found to be increased in patients with COVID-19. Furthermore, this increase occurred progressively with the severity of the condition. In addition, some studies reported that IL-10 levels increased earlier than those of IL-6 in the blood of critically ill patients [22] . As a pro-inflammatory cytokine, IL-6 is commonly increased in sepsis, acute respiratory distress syndrome, and in major burns [28] . 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