In Vitro Wound Healing Improvement By Low-level Laser Therapy Application In Cultured Gingival Fibroblasts

The aim of this study was to determine adequate energy doses using specific parameters of LLLT to produce biostimulatory effects on human gingival fibroblast culture. Cells (3 10 4 cells/cm 2) were seeded on 24-well acrylic plates using plain DMEM supplemented with 10 fetal bovine serum. After 48-hour incubation with 5 CO2 at 37C, cells were irradiated with a InGaAsP diode laser prototype (LASERTable; 780 3 nm; 40mW) with energy doses of 0.5, 1.5, 3, 5, and 7J/cm 2. Cells were irradiated every 24h totalizing 3 applications. Twenty-four hours after the last irradiation, cell metabolism was evaluated by the MTT assay and the two most effective doses (0.5 and 3J/cm 2) were selected to evaluate the cell number (trypan blue assay) and the cell migration capacity (wound healing assay; transwell migration assay). Data were analyzed by the Kruskal-Wallis and Mann-Whitney nonparametric tests with statistical significance of 5. Irradiation of the fibroblasts with 0.5 and 3J/cm 2 resulted in significant increase in cell metabolism compared with the nonrradiated group (P 0.05). Both energy doses promoted significant increase in the cell number as well as in cell migration (P 0.05). These results demonstrate that, under the tested conditions, LLLT promoted biostimulation of fibroblasts in vitro. Copyright © 2012 Fernanda G. Basso et al.Hkkinen, L., Uitto, V.J., Larjava, H., Cell biology of gingival wound healing (2000) Periodontology 2000, 24 (1), pp. 127-152Kreisler, M., Christoffers, A.B., Al-Haj, H., Willershausen, B., D'Hoedt, B., Low level 809-nm diode laser-induced in vitro stimulation of the proliferation of human gingival fibroblasts (2002) Lasers in Surgery and Medicine, 30 (5), pp. 365-369. , DOI 10.1002/lsm.10060Posten, W., Wrone, D.A., Dover, J.S., Arndt, K.A., Silapunt, S., Alam, M., Low-level laser therapy for wound healing: Mechanism and efficacy (2005) Dermatologic Surgery, 31 (3), pp. 334-340Saygun, I., Karacay, S., Serdar, M., Ural, A.U., Sencimen, M., Kurtis, B., Effects of laser irradiation on the release of basic fibroblast growth factor (bFGF), insulin like growth factor-1 (IGF-1), and receptor of IGF-1 (IGFBP3) from gingival fibroblasts (2008) Lasers in Medical Science, 23 (2), pp. 211-215. , DOI 10.1007/s10103-007-0477-3Skopin, M.D., Molitor, S.C., Effects of near-infrared laser exposure in a cellular model of wound healing (2009) Photodermatology Photoimmunology and Photomedicine, 25 (2), pp. 75-80Hakki, S.S., Bozkurt, S.B., Effects of different setting of diode laser on the mRNA expression of growth factors and type i collagen of human gingival fibroblasts (2012) Lasers in Medical Science, 27 (2), pp. 325-331Peplow, P.V., Chung, T.Y., Baxter, G.D., Laser photobiomodulation of proliferation of cells in culture: A review of human and animal studies (2010) Photomedicine and Laser Surgery, 28, pp. 3-S40. , supplement 1Basso, F.G., Oliveira, C.F., Kurachi, C., Hebling, J., Costa, C.A., Biostimulatory effect of low-level laser therapy on keratinocytes in vitro Lasers in Medical Science, , In pressOliveira, C.F., Basso, F.G., Lins, E.C., Kurachi, C., Hebling, J., Bagnato, V.S., De Souza Costa, C.A., In vitro effect of low-level laser on odontoblast-like cells (2011) Laser Physics Letters, 8 (2), pp. 155-163Mosmann, T., Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays (1983) Journal of Immunological Methods, 65 (1-2), pp. 55-63Wiegand, C., Hipler, U., Methods for the measurement of cell and tissue compatibility including tissue regeneration process (2008) GMS Krankenhaushygiene Interdisziplinr, 3 (1), pp. 1863-5245Hoang, A.M., Oates, T.W., Cochran, D.L., In vitro wound healing responses to enamel matrix derivative (2000) Journal of Periodontology, 71 (8), pp. 1270-1277Liang, C.-C., Park, A.Y., Guan, J.-L., In vitro scratch assay: A convenient and inexpensive method for analysis of cell migration in vitro (2007) Nature Protocols, 2 (2), pp. 329-333. , DOI 10.1038/nprot.2007.30, PII NPROT.2006.30Cceres, M., Romero, A., Copaja, M., Daz-Araya, G., Martnez, J., Smith, P.C., Simvastatin alters fibroblastic cell responses involved in tissue repair (2011) Journal of Periodontal Research, 46 (4), pp. 456-463Chor, A., De Azevedo, A.M., Maiolino, A., Nucci, M., Successful treatment of oral lesions of chronic lichenoid graft-vs.-host disease by the addition of low-level laser therapy to systemic immunosuppression (2004) European Journal of Haematology, 72 (3), pp. 222-224. , DOI 10.1046/j.0902-4441.2003.00202.xAbramoff, M.M.F., Lopes, N.N.F., Lopes, L.A., Dib, L.L., Guilherme, A., Caran, E.M., Barreto, A.D., Petrilli, A.S., Low-level laser therapy in the prevention and treatment of chemotherapy-induced oral mucositis in young patients (2008) Photomedicine and Laser Surgery, 26 (4), pp. 393-400Woodruff, L.D., Bounkeo, J.M., Brannon, W.M., Dawes Jr., K.S., Barham, C.D., Waddell, D.L., Enwemeka, C.S., The efficacy of laser therapy in wound repair: A meta-analysis of the literature (2004) Photomedicine and Laser Surgery, 22 (3), pp. 241-247. , DOI 10.1089/1549541041438623Damante, C.A., De Micheli, G., Miyagi, S.P.H., Feist, I.S., Marques, M.M., Effect of laser phototherapy on the release of fibroblast growth factors by human gingival fibroblasts (2009) Lasers in Medical Science, 24 (6), pp. 885-891Almeida-Lopes, L., Rigau, J., Zangaro, R.A., Guidugli-Neto, J., Jaeger, M.M.M., Comparison of the low level laser therapy effects on cultured human gingival fibroblasts proliferation using different irradiance and same fluence (2001) Lasers in Surgery and Medicine, 29 (2), pp. 179-184. , DOI 10.1002/lsm.1107Alghamdi, K.M., Kumar, A., Moussa, N.A., Low-level laser therapy: A useful technique for enhancing the proliferation of various cultured cells (2011) Lasers in Medical Science, 27 (1), pp. 237-249Gao, X., Xing, D., Molecular mechanisms of cell proliferation induced by low power laser irradiation (2009) Journal of Biomedical Science, 164Karu, T.I., Pyatibrat, L.V., Kolyakov, S.F., Afanasyeva, N.I., Absorption measurements of a cell monolayer relevant to phototherapy: Reduction of cytochrome c oxidase under near IR radiation (2005) Journal of Photochemistry and Photobiology B: Biology, 81 (2), pp. 98-106. , DOI 10.1016/j.jphotobiol.2005.07.002, PII S1011134405001302Eells, J.T., Henry, M.M., Summerfelt, P., Wong-Riley, M.T.T., Buchmann, E.V., Kane, M., Whelan, N.T., Whelan, H.T., Therapeutic photobiomodulation for methanol-induced retinal toxicity (2003) Proceedings of the National Academy of Sciences of the United States of America, 100 (6), pp. 3439-3444. , DOI 10.1073/pnas.0534746100Zhang, L., Xing, D., Gao, X., Wu, S., Low-power laser irradiation promotes cell proliferation by activating PI3K/Akt pathway (2009) Journal of Cellular Physiology, 219 (3), pp. 553-562Azevedo, L.H., De Paula Eduardo, F., Moreira, M.S., De Paula Eduardo, C., Marques, M.M., Influence of different power densities of LILT on cultured human fibroblast growth: A pilot study (2006) Lasers in Medical Science, 21 (2), pp. 86-89. , DOI 10.1007/s10103-006-0379-9Lagan, K.M., Alyson Clements, B., McDonough, S., David Baxter, G., Low intensity laser therapy (830nm) in the management of minor postsurgical wounds: A controlled clinical study (2001) Lasers in Surgery and Medicine, 28 (1), pp. 27-32. , DOI 10.1002/1096-9101(2 001)28:13.0.CO;2-

Cytotoxic Effects Of Zoledronic Acid On Human Epithelial Cells And Gingival Fibroblasts

Bisphosphonate-induced osteonecrosis has been related to the cytotoxicity of these drugs on oral mucosa cells. A previous study showed that 5 μM of zoledronic acid (ZA), a nitrogen-containing bisphosphonate, is the highest concentration of this drug found in the oral cavity of patients under treatment. Therefore, in order to simulate an osteonecrosis clinical condition, the aim of this study was to evaluate the highest concentration of ZA applied on human epithelial cells (HaCaT) and gingival fibroblasts. For this purpose, cells (3x104 cells/cm2) were seeded in wells for 48 h using complete culture medium (cDMEM). After 48 h incubation, the cDMEM was replaced by fresh serum-free culture medium (DMEM-FBS) in which the cells were maintained for additional 24 h. Then, 5 μM ZA were added to the DMEM-FBS and the cells incubated in contact with the drug for 48 h. After this period, the number of viable cells (trypan blue), cell viability (MTT assay), total protein (TP) production and cell morphology (SEM analysis) were assessed. Data were analyzed statistically by Mann-Whitney, ANOVA and Tukey's test (α=0.05). ZA caused a significant reduction in the number of viable cells and decreased the metabolic activity of both cell lines. However, decrease of TP production occurred only in the epithelial cell cultures. Morphological alterations were observed in both cell types treated with ZA. In conclusion, ZA (5 μM) was cytotoxic to human epithelial cells and gingival fibroblast cultures, which could be associated, clinically, with the development of bisphosphonateinduced osteonecrosis.246551558Civitelli, R., Napoli, N., Armamento-Villareal, R., Use of intravenous bisphosphonates in osteoporosis (2007) Curr Osteoporos Rep, 5, pp. 8-13Cohen, S.B., An update on bisphosphonates (2004) Curr Rheumatol Rep, 6, pp. 59-65Rogers, M.J., Watts, D.J., Russel, R.G., Overview of bisphosphonates (1997) Cancer, 80, pp. 1652-1660Rogers, M.J., Gordon, S., Benford, H.L., Coxon, F.P., Luckman, S.P., Monkkonen, J., Cellular and molecular mechanisms of action of bisphosphonates (2000) Cancer Supl, 88, pp. 2961-2978Lawson, M.A., Xia, Z., Barnett, B.L., Triffitt, J.T., Phipps, R.J., Dunford, J.E., Differences between bisphosphonates in binding affinities for hydroxyapatite (2010) J Biomed Mater Res Part B: Appl Biomater, 92, pp. 149-155Allen, M.R., Burr, D.B., The pathogenesis of bisphosphonate-related osteonecrosis of the jaw: So many hypotheses, so few data (2009) J Oral Maxillofac Surg, 67, pp. 61-70Otto, S., Pautke, C., Opelz, C., Wesphal, I., Drosse, I., Swager, J., Osteonecrosis of the jaw: Effects of bisphosphonate type, local concentration, and acidic milieu on the pathomechanism (2010) J Oral Maxillofac Surg, 68, pp. 2837-2845Reid, I.R., Booland, M.J., Is bisphosphonate-associated osteonecrosis of the jaw caused by soft tissue toxicity? (2007) Bone, 41, pp. 318-320Scheper, M.A., Badros, A., Chausparat, R., Cullen, K.J., Meiller, T.F., Effect of zoledronic acid on oral fibroblasts and epithelial cells: A potential mechanism of bisphosphonate-associated osteonecrosis (2009) Br J Haematol, 144, pp. 667-676Scheper, M.A., Badros, A., Salama, A.R., Wartburton, G., Cullen, K.J., Weikel, D.S., A novel bioassay model to determine clinically significant bisphosphonate levels (2009) Support Care Cancer, 17, pp. 1553-1557Ruggiero, S.L., Mehrotra, B., Rosenberg, T.J., Engroff, S.L., Osteonecrosis of the jaws associated with the use of bisphosphonates: A review of 63 cases (2004) J Oral Maxillofac Surg, 62, pp. 527-534Walter, C., Klein, M.O., Pabst, A., Al-Nawas, B., Duscher, H., Ziebart, T., Influence of bisphosphonates on endothelial cells, fibroblasts, and osteogenic cells (2010) Clin Oral Investig, 14, pp. 35-41Kumar, S.K.S., Gorur, A., Schaauddin, C., Shuler, C.F., Costerton, J.W., Sedghizadeh, P.P., The role of microbial biofilms in osteonecrosis of the jaw associated with bisphosphonate therapy (2010) Curr Osteoporos Rep, 8, pp. 40-48Aas, J.A., Paster, B.J., Stokes, L.N., Olsen, I., Dewhirst, F.E., Defining the normal bacterial flora of the oral cavity (2005) J Clin Microbiol, 43, pp. 5721-5732Basso, F.G., Pansani, T.N., Turrioni, A.P.S., Bagnato, V.S., Hebling, J., de Souza Costa, C.A., In vitro wound healing improvement by low-level laser therapy application in cultured gingival fibroblasts (2012) Int J Dent, , [Epub ahead of print. DOI: 10.1155/2012/719452]Wiegand, C., Hipler, U., Methods for the measurement of cell and tissue compatibility including tissue regeneration process (2008) GMS Krankenhhyg Interdiszip, 3, pp. 1863-5245Basso, F.G., Oliveira, C.F., Kurachi, C., Hebling, J., de Souza Costa, C.A., Biostimulatory effect of low-level laser therapy on keratinocytes in vitro (2013) Lasers Med Sci, 28, pp. 367-374De Souza Costa, C.A., Duarte, P.T., de Souza, P.P., Giro, E.M., Hebling, J., Cytotoxic effects and pulpal response caused by a mineral trioxide aggregate formulation and calcium hydroxide (2008) Am J Dent, 21, pp. 255-261Oliveira, C.F., Basso, F.G., Lins, E.C.C., Kurachi, C., Hebling, J., Bagnato, V.S., Increased viability of odontoblast-like cells subjected to low-level laser irradiation (2010) Laser Phys, 20, pp. 1659-1666Read, S.M., Northcote, D.H., Minimization of variation in the response to different proteins of the Coomassie blue G dye-binding assay for protein (1981) Anal Biochem, 116, pp. 53-64Oliveira, C.F., Basso, F.G., Lins, E.C., Kurachi, C., Hebling, J., Bagnato, V.S., In vitro effect of low-level laser on odontoblast-like cells (2011) Laser Phys Lett, 8, pp. 155-163Simon, M.J.K., Niehoff, P., Kimming, B., Wiltfang, J., Açil, Y., Expression profile and synthesis of different collagen types I, II III and V of human gingival fibroblasts, osteoblasts, ans SaOs-2 cells after bisphosphonate treatment (2010) Clin Oral Investig, 14, pp. 51-58Migliorati, C.A., Siegel, M.A., Elting, L.S., Bisphosphonate-associated osteonecrosis: A long-term complication of bisphosphonate treatment (2006) Lancet Oncol, 7, pp. 508-514Werner, S., Krieg, T., Smola, H., Keratinocyte-fibroblast interactions in wound healing (2007) J Investigative Dermatol, 127, pp. 998-1008Ravosa, M.J., Ning, J., Liu, Y., Stack, M.S., Bisphosphonate effects on the behavior of oral epithelial cells and oral fibroblasts (2011) Arch Oral Biol, 56, pp. 491-49

In Vitro Effect Of Low-level Laser Therapy On Typical Oral Microbial Biofilms

The aim of this study was to evaluate the effect of specific parameters of low-level laser therapy (LLLT) on biofilms formed by Streptococcus mutans, Candida albicans or an association of both species. Single and dual-species biofilms - SSB and DSB - were exposed to laser doses of 5, 10 or 20 J/cm 2 from a near infrared InGaAsP diode laser prototype (LASERTable; 780 ± 3 nm, 0.04 W). After irradiation, the analysis of biobilm viability (MTT assay), biofilm growth (cfu/mL) and cell morphology (SEM) showed that LLLT reduced cell viability as well as the growth of biofilms. The response of S. mutans (SSB) to irradiation was similar for all laser doses and the biofilm growth was dose dependent. However, when associated with C. albicans (DSB), S. mutans was resistant to LLLT. For C. albicans, the association with S. mutans (DSB) caused a significant decrease in biofilm growth in a dose-dependent fashion. The morphology of the microorganisms in the SSB was not altered by LLLT, while the association of microbial species (DSB) promoted a reduction in the formation of C. albicans hyphae. LLLT had an inhibitory effect on the microorganisms, and this capacity can be altered according to the interactions between different microbial species.226502510Marques, M.M., Pereira, A.N., Fujihara, N.A., Nogueira, F.N., Eduardo, C.P., Effect of low-power laser irradiation on protein synthesis and ultrastructure of human gingival fibroblasts (2004) Lasers Surg Med, 34, pp. 260-265Damante, C.A., de Micheli, G., Miyagi, S.P.H., Feist, I.S., Marques, M.M., Effect of laser phototherapy on the release of fibroblast growth factors by human gingival fibroblasts (2009) Lasers Med Sci, 24, pp. 885-891Moritz, A., Schoop, U., Goharkhay, K., Schauer, P., Doertbudak, O., Wernisch, J., Treatment of periodontal pockets with a diode laser (1998) Lasers Surg Med, 22, pp. 302-311Nussbaum, E.L., Lilge, L., Mazzulli, T., Effects of 630-, 660-, 810-, and 905-nm laser irradiation delivering radiant exposure of 1-50 J/cm 2 on three species of bacteria in vitro (2002) J Clin Laser Med Surg, 20, pp. 325-333Nussbaum, E.L., Lilge, L., Mazzulli, T., Effects of low-level laser therapy (LLLT) of 810 nm upon in vitro growth of bacteria: Relevance of irradiance and radiant exposure (2003) J Clin Laser Med Surg, 21, pp. 283-290Lino, M.D.M.C., Carvalho, F.B., Oliveira, L.R., Magalhães, E.B., Pinheiro, A.L.B., Ramalho, L.M.P., Laser phototherapy as a treatment for radiotherapy-induced oral mucositis (2011) Braz Dent J, 22, pp. 162-165Maver-Biscanin, M., Mravak-Stipetic, M., Jerolimov, V., Biscanin, A., Fungicidal effect of diode laser irradiation in patients with denture stomatitis (2004) Lasers Surg Med, 35, pp. 259-262Dworkin, M., Endogenous photosensitization in a carotinoidless mutant of Rhodopseudomonas speroides (1958) J Gen Physiol, 43, pp. 1099-1112Rosenberg, B., Kemeny, G., Switzer, R.C., Hamilton, T.C., Quantitative evidence for protein denaturation as the cause of thermal death (1971) Nature, 232, pp. 471-473Krespi, Y.P., Kizhner, V., Nistico, L., Hall-Stoodley, L., Stoodley, P., Laser disruption and killing of methicillin-resistant Staphylococcus aureus biofilms (2011) Am J Otolaryngol, 32, pp. 198-202Shirtliff, M.E., Peters, B.M., Jabra-Rizk, M.A., Cross-kingdom interactions: Candida albicans and bacteria (2009) FEMS Microbiol Lett, 299, pp. 1-8Pereira-Cenci, T., Deng, D.M., Kraneveld, E.A., Manders, E.M.M., del Bel, C.A.A., ten Cate, J.M., The effect of Streptococcus mutans and Candida glabrata on Candida albicans biofilms formed on different surfaces (2008) Arch Oral Biol, 53, pp. 755-764Marsh, P.D., Microbial ecology of dental plaque and its significance in health and disease (1994) Adv Dent Res, 8, pp. 263-271Karkowska-Kuleta, J., Rapala-Kozik, M., Kozik, A., Fungi pathogenic to humans: Molecular bases of virulence of Candida albicans, Cryptococcus neoformans and Aspergillus fumigatus (2009) Acta Biochim Pol, 56, pp. 211-224Thein, Z.M., Samaranayake, Y.H., Samaranayake, L.P., Dietary sugars, serum and the biocide chlorhexidine digluconate modify the population and structural dynamics of mixed Candida albicans and Escherichia coli biofilms (2007) APMIS, 115, pp. 1241-1251Kwieciński, J., Eick, S., Wójcik, K., Effects of tea tre (Melaleuca alternifolia) oil on Staphylococcus aureus in biofilms and stationary phase (2009) Int J Antimicrob Agents, 33, pp. 343-347Wang, Z.C., Fan, L.Y., Jiang, J.Q., Cai, W., Ding, Y., Study on the counting of Streptococcus mutans, Streptococcus sanguis, Haemophilus actinomycetemcomitans by methyl thiazolyl tetrazolium colorimetric method (2010) Hua Xi Kou Qiang Yi Xue Za Zhi, 28, pp. 306-310Nguyen, P.T.M., Abranches, J., Phan, T., Marquis, R.E., Repressed respiration of oral Streptococci grow in biofilms (2002) Curr Microbiol, 44, pp. 262-266Singleton, S., Treloar, R., Warren, P., Watson, G.K., Hodgson, R., Allison, C., Methods for microscopic characterization of oral biofilms: Analysis of colonization, microstructure, and molecular transport phenomena (1997) Adv Dent Res, 11, pp. 133-149Jarosz, L.M., Deng, D.M., van der Mei, H.C., Crielaard, W., Krom, B.P., Streptococcus mutans competence-stimulating peptide inhibits Candida albicans hypha formation (2009) Eukaryot Cell, 8, pp. 1658-1664Dortbudak, O., Haas, R., Bernhart, T., Mailath-Pokorny, G., Lethal photosensitization for decontamination of implant surface in the treatment of peri-implantitis (2001) Clin Oral Implant Res, 12, pp. 104-10

Combined low densities of FoxP3+ and CD3+ tumor-infiltrating lymphocytes identify stage II colorectal cancer at high risk of progression

The densities of CD3+ and CD8+ tumor-infiltrating lymphocytes (TILs), combined with TNM (tumor-node-metastasis) staging, have prognostic value for nonmetastatic colorectal cancer (CRC) patients. We compared the prognostic value of CD3+ and FoxP3+ TILs at the invasive front, TNM classifiers, and microsatellite (MS) status in a trial set of patients with stage II-III CRC (n = 413), by recursive partitioning with a classification and regression tree (CART). Significant prognostic factors and interactions were re-assessed by logistic regression and Cox proportional-hazards modeling in the trial and a validation set (n = 215) of patients with stage II CRC. In the trial set, CART indicated that TIL numbers were of value only in predicting recurrence risk for stage II cancers, where low densities of FoxP3+ TILs ranked first and low densities of CD3+ TILs further stratifiying risk. Multivariate analysis showed that TILs interacted with tumor stage (FoxP3+, P = 0.06; CD3+, P = 0.02) and MS instability (FoxP3+; P = 0.02). In stage II MS-stable cancers, concomitant low densities of both FoxP3+ and CD3+ TILs identified patients with the highest progression risk in the trial (HR 7.24; 95%CI, 3.41-15.4; P < 0.001) and the validation (HR 15.16; 95% IC, 3.43-66.9; P < 0.001) sets. FoxP3+ and CD3+ TIL load in CRC was more informative than other prognostic factors before the cancer progressed to lymph nodes. This prognostic information about TILs, including FoxP3+ cells, suggests that randomized controlled trials might be refined to include interactions between TNM status, molecular classifiers, and post-surgical treatments

Search for flavour-changing neutral currents in processes with one top quark and a photon using 81 fb⁻¹ of pp collisions at \sqrts = 13 TeV with the ATLAS experiment

A search for flavour-changing neutral current (FCNC) events via the coupling of a top quark, a photon, and an up or charm quark is presented using 81 fb−1 of proton–proton collision data taken at a centre-of-mass energy of 13 TeV with the ATLAS detector at the LHC. Events with a photon, an electron or muon, a b-tagged jet, and missing transverse momentum are selected. A neural network based on kinematic variables differentiates between events from signal and background processes. The data are consistent with the background-only hypothesis, and limits are set on the strength of the tqγ coupling in an effective field theory. These are also interpreted as 95% CL upper limits on the cross section for FCNC tγ production via a left-handed (right-handed) tuγ coupling of 36 fb (78 fb) and on the branching ratio for t→γu of 2.8×10−5 (6.1×10−5). In addition, they are interpreted as 95% CL upper limits on the cross section for FCNC tγ production via a left-handed (right-handed) tcγ coupling of 40 fb (33 fb) and on the branching ratio for t→γc of 22×10−5 (18×10−5). © 2019 The Author(s

Search for heavy resonances decaying into a Z or W boson and a Higgs boson in final states with leptons and b-jets in 139 fb−1 of pp collisions at s√ = 13 TeV with the ATLAS detector

This article presents a search for new resonances decaying into a Z or W boson and a 125 GeV Higgs boson h, and it targets the νν¯¯¯bb¯¯, ℓ+ℓ−bb¯¯, or ℓ±νbb¯¯ final states, where ℓ = e or μ, in proton-proton collisions at s√ = 13 TeV. The data used correspond to a total integrated luminosity of 139 fb−1 collected by the ATLAS detector during Run 2 of the LHC at CERN. The search is conducted by examining the reconstructed invariant or transverse mass distributions of Zh or Wh candidates for evidence of a localised excess in the mass range from 220 GeV to 5 TeV. No significant excess is observed and 95% confidence-level upper limits between 1.3 pb and 0.3 fb are placed on the production cross section times branching fraction of neutral and charged spin-1 resonances and CP-odd scalar bosons. These limits are converted into constraints on the parameter space of the Heavy Vector Triplet model and the two-Higgs-doublet model

Search for boosted diphoton resonances in the 10 to 70 GeV mass range using 138 fb−1 of 13 TeV pp collisions with the ATLAS detector

A search for diphoton resonances in the mass range between 10 and 70 GeV with the ATLAS experiment at the Large Hadron Collider (LHC) is presented. The analysis is based on pp collision data corresponding to an integrated luminosity of 138 fb−1 at a centre-of-mass energy of 13 TeV recorded from 2015 to 2018. Previous searches for diphoton resonances at the LHC have explored masses down to 65 GeV, finding no evidence of new particles. This search exploits the particular kinematics of events with pairs of closely spaced photons reconstructed in the detector, allowing examination of invariant masses down to 10 GeV. The presented strategy covers a region previously unexplored at hadron colliders because of the experimental challenges of recording low-energy photons and estimating the backgrounds. No significant excess is observed and the reported limits provide the strongest bound on promptly decaying axion-like particles coupling to gluons and photons for masses between 10 and 70 GeV

Evidence for the charge asymmetry in pp → tt¯ production at s√ = 13 TeV with the ATLAS detector

Inclusive and differential measurements of the top–antitop (tt¯) charge asymmetry Att¯C and the leptonic asymmetry Aℓℓ¯C are presented in proton–proton collisions at s√ = 13 TeV recorded by the ATLAS experiment at the CERN Large Hadron Collider. The measurement uses the complete Run 2 dataset, corresponding to an integrated luminosity of 139 fb−1, combines data in the single-lepton and dilepton channels, and employs reconstruction techniques adapted to both the resolved and boosted topologies. A Bayesian unfolding procedure is performed to correct for detector resolution and acceptance effects. The combined inclusive tt¯ charge asymmetry is measured to be Att¯C = 0.0068 ± 0.0015, which differs from zero by 4.7 standard deviations. Differential measurements are performed as a function of the invariant mass, transverse momentum and longitudinal boost of the tt¯ system. Both the inclusive and differential measurements are found to be compatible with the Standard Model predictions, at next-to-next-to-leading order in quantum chromodynamics perturbation theory with next-to-leading-order electroweak corrections. The measurements are interpreted in the framework of the Standard Model effective field theory, placing competitive bounds on several Wilson coefficients

Search for single vector-like B quark production and decay via B → bH(b¯b) in pp collisions at √s = 13 TeV with the ATLAS detector

A search is presented for single production of a vector-like B quark decaying into a Standard Model b-quark and a Standard Model Higgs boson, which decays into a b¯b pair. The search is carried out in 139 fb−1 of √s = 13 TeV proton-proton collision data collected by the ATLAS detector at the LHC between 2015 and 2018. No significant deviation from the Standard Model background prediction is observed, and mass-dependent exclusion limits at the 95% confidence level are set on the resonance production cross-section in several theoretical scenarios determined by the couplings cW, cZ and cH between the B quark and the Standard Model W, Z and Higgs bosons, respectively. For a vector-like B occurring as an isospin singlet, the search excludes values of cW greater than 0.45 for a B resonance mass (mB) between 1.0 and 1.2 TeV. For 1.2 TeV < mB < 2.0 TeV, cW values larger than 0.50–0.65 are excluded. If the B occurs as part of a (B, Y) doublet, the smallest excluded cZ coupling values range between 0.3 and 0.5 across the investigated resonance mass range 1.0 TeV < mB < 2.0 TeV