Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where S. Khoo is active.

Publication


Featured researches published by S. Khoo.


European Respiratory Journal | 2011

Association between human rhinovirus C and severity of acute asthma in children

Joelene Bizzintino; Wai-Ming Lee; Ingrid A. Laing; F. Vang; T. Pappas; Guicheng Zhang; Andrew C. R. Martin; S. Khoo; Desmond Cox; Gary C. Geelhoed; P.C. Mcminne; Jack Goldblatt; James E. Gern; P. N. Le Souëf

A new and potentially more pathogenic group of human rhinovirus (HRV), group C (HRVC), has recently been discovered. We hypothesised that HRVC would be present in children with acute asthma and cause more severe attacks than other viruses or HRV groups. Children with acute asthma (n = 128; age 2–16 yrs) were recruited on presentation to an emergency department. Asthma exacerbation severity was assessed, and respiratory viruses and HRV strains were identified in a nasal aspirate. The majority of the children studied had moderate-to-severe asthma (85.2%) and 98.9% were admitted to hospital. HRV was detected in 87.5% and other respiratory viruses in 14.8% of children, most of whom also had HRV. HRVC was present in the majority of children with acute asthma (59.4%) and associated with more severe asthma. Children with HRVC (n = 76) had higher asthma severity scores than children whose HRV infection was HRVA or HRVB only (n = 34; p = 0.018), and all other children (n = 50; p = 0.016). Of the 19 children with a non-HRV virus, 13 had HRV co-infections, seven of these being HRVC. HRVC accounts for the majority of asthma attacks in children presenting to hospital and causes more severe attacks than previously known HRV groups and other viruses.


American Journal of Respiratory and Critical Care Medicine | 2013

Human Rhinovirus Species C Infection in Young Children with Acute Wheeze Is Associated with Increased Acute Respiratory Hospital Admissions

Des W. Cox; Joelene Bizzintino; Giovanni Ferrari; S. Khoo; Guicheng Zhang; S. Whelan; Wai-Ming Lee; Yury A. Bochkov; Gary C. Geelhoed; J. Goldblatt; James E. Gern; Ia Laing; P. N. Le Souëf

RATIONALE Human rhinovirus species C (HRV-C) is the most common cause of acute wheezing exacerbations in young children presenting to hospital, but its impact on subsequent respiratory illnesses has not been defined. OBJECTIVES To determine whether acute wheezing exacerbations due to HRV-C are associated with increased hospital attendances due to acute respiratory illnesses (ARIs). METHODS Clinical information and nasal samples were collected prospectively from 197 children less than 5 years of age, presenting to hospital with an acute wheezing episode. Information on hospital attendances with an ARI before and after recruitment was subsequently obtained. MEASUREMENTS AND MAIN RESULTS HRV was the most common virus identified at recruitment (n = 135 [68.5%]). From the 120 (88.9%) samples that underwent typing, HRV-C was the most common HRV species identified, present in 81 (67.5%) samples. Children with an HRV-related wheezing illness had an increased risk of readmission with an ARI (relative risk, 3.44; 95% confidence interval, 1.17-10.17; P = 0.03) compared with those infected with any other virus. HRV-C, compared with any other virus, was associated with an increased risk of a respiratory hospital admission before (49.4% vs. 27.3%, respectively; P = 0.004) and within 12 months (34.6% vs. 17.0%; P = 0.01) of recruitment. Risk for subsequent ARI admissions was further increased in atopic subjects (relative risk, 6.82; 95% confidence interval, 2.16-21.55; P = 0.001). Admission risks were not increased for other HRV species. CONCLUSIONS HRV-C-related wheezing illnesses were associated with an increased risk of prior and subsequent hospital respiratory admissions. These associations are consistent with HRV-C causing recurrent severe wheezing illnesses in children who are more susceptible to ARIs.


Clinical & Experimental Allergy | 2004

β2 adrenoceptor Arg16Gly polymorphism, airway responsiveness, lung function and asthma in infants and children

Steve Turner; S. Khoo; Ingrid A. Laing; Lyle J. Palmer; Neil A. Gibson; Peter J. Rye; Lou I. Landau; Jack Goldblatt; P. N. Le Souëf

Background We have previously reported a relationship between increased airway responsiveness (AR) in infancy and reduced childhood lung function.


Clinical and Vaccine Immunology | 2006

Association of CD14 promoter polymorphism with otitis media and pneumococcal vaccine responses.

Selma P. Wiertsema; S. Khoo; Gareth Baynam; Reinier H. Veenhoven; Ingrid A. Laing; G. A. Zielhuis; Ger T. Rijkers; J. Goldblatt; Peter N. LeSouëf; Elisabeth A. M. Sanders

Innate immunity is of particular importance for protection against infection during early life, when adaptive immune responses are immature. CD14 plays key roles in innate immunity, including in defense against pathogens associated with otitis media, a major pediatric health care issue. The T allele of the CD14 C-159T polymorphism has been associated with increased serum CD14 levels. Our objective was to investigate the hypothesis that the CD14 C-159T allele is protective against recurrent acute otitis media in children. The association between the CD14 promoter genotype and the number of acute otitis media episodes was evaluated both retrospectively and prospectively in a cohort of 300 children. Serotype-specific immunoglobulin G (IgG) antibody responses after pneumococcal vaccinations were examined according to CD14 genotype to compare immune responsiveness across genotypes. An age-dependent association was found: compared with that for CC homozygotes aged between 12 to 24 months, TT homozygotes had fewer episodes of acute otitis media (79 versus 41%, respectively; P = 0.004); this relationship was absent in older children. Additionally, TT homozygotes showed higher serotype-specific anti-pneumococcal IgG antibody levels. Our data suggest that genetic variation in CD14, a molecule at the interface of innate and adaptive immune responses, plays a key role in the defense against middle ear disease in childhood and in pneumococcal vaccine responsiveness. These findings are likely to be important to these and other immune-mediated outcomes in early life.


Allergy | 2009

Opposite gene by environment interactions in Karelia for CD14 and CC16 single nucleotide polymorphisms and allergy

Guicheng Zhang; S. Khoo; Tiina Laatikainen; P. T. Pekkarinen; Erkki Vartiainen; L. von Hertzen; Catherine M. Hayden; Jack Goldblatt; Mika J. Mäkelä; Tari Haahtela; P. N. Le Souëf

Background:  Finnish Karelians have a higher prevalence of allergic disease than Russian Karelians. As both populations are generally from the same ethnic group, the Karelian population offers a unique opportunity to analyse genetic and allergic disease interactions between ‘Western’ and ‘Eastern’ environments.


Clinical & Experimental Allergy | 2009

Anti-bacterial IgE in the antibody responses of house dust mite allergic children convalescent from asthma exacerbation

Belinda J. Hales; Andrew C. R. Martin; Leigh J. Pearce; Kristina Rueter; Guicheng Zhang; S. Khoo; Catherine M. Hayden; Joelene Bizzintino; P. McMinn; Gary C. Geelhoed; Wai-Ming Lee; Jack Goldblatt; Ingrid A. Laing; Peter N. LeSouëf; Wayne R. Thomas

Background Atopic sensitization to the house dust mite (HDM) is associated with altered antibody responses to the nasopharyngeal colonizing bacterium Haemophilus influenzae and children admitted to the emergency department for asthma exacerbation have reduced IgG responses to HDM allergens.


Allergy | 2010

The importance of environment on respiratory genotype/phenotype relationships in the Inuit.

Pierre Candelaria; Vibeke Backer; S. Khoo; Joelene Bizzintino; Catherine M. Hayden; Gareth Baynam; Ingrid A. Laing; Guicheng Zhang; Celeste Porsbjerg; Jack Goldblatt; P. N. Le Souëf

To cite this article: Candelaria PV, Backer V, Khoo S‐K, Bizzintino JA, Hayden CM, Baynam G, Laing IA, Zhang G, Porsbjerg C, Goldblatt J, LeSouëf PN, The Greenlandic Study Population Group. The importance of environment on respiratory genotype/phenotype relationships in the Inuit. Allergy 2010; 65: 229–237.


Clinical & Experimental Allergy | 2015

Lower anti-echovirus antibody responses in children presenting to hospital with asthma exacerbations

Jua Iwasaki; L. Y. Chai; S. Khoo; Joelene Bizzintino; Ingrid A. Laing; P. N. Le Souëf; Wayne R. Thomas; Belinda J. Hales

Rhinoviruses from the Enterovirus genus cause frequent infections and induce remarkably high titres of anticapsid antigen antibodies in asthmatics, while the prevalence of neutralising antibodies to the gut‐trophic echoviruses from the same genus is diminished.


Clinical & Experimental Allergy | 2017

High fractional exhaled nitric oxide and sputum eosinophils are associated with an increased risk of future virus-induced exacerbations: A prospective cohort study

Asger Bjerregaard; Ingrid A. Laing; Vibeke Backer; Asger Sverrild; S. Khoo; Glenys Chidlow; Chisha Sikazwe; David William Smith; P. N. Le Souëf; Celeste Porsbjerg

The major trigger of asthma exacerbations is infection with a respiratory virus, most commonly rhinovirus. Type 2 inflammation is known to be associated with an increased risk of exacerbations in general. Whether type 2 inflammation at baseline increases the risk of future virus‐induced exacerbations is unknown.


International Journal of Pediatrics and Child Health | 2015

Recurrent rhinovirus detections in children following a rhinovirus-induced wheezing exacerbation: A retrospective study

S. Hurdum; Guicheng Zhang; S. Khoo; Joelene Bizzintino; K. Franks; K. Lindsay; Anthony D. Keil; Desmond Cox; J. Goldblatt; Yury A. Bochkov; James E. Gern; C. Ulrik; P. Le Souef; Ia Laing

INTRODUCTION It is unclear if children with a rhinovirus (RV)-induced wheezing exacerbation are more susceptible to viruses longitudinally, and whether a parental history of asthma and/or allergy impacts their susceptibility. The objective of this study was to determine if RV, RV-A and RV-C related wheezing exacerbations in children were associated with prior or subsequent viral detections and investigate the role of parental history of asthma and allergy. MATERIALS AND METHODS Children presenting to hospital with acute wheeze were prospectively recruited and tested for respiratory viruses. Data on viruses detected in other respiratory samples (May 1997 to December 2012) were collected from hospital microbiology records and additional RV testing was performed on stored hospital respiratory samples (September 2009 to December 2012). A positive parental history was defined as either parent with self-reported asthma and/or allergy. RESULTS At recruitment, RV was detected in 69.2% of samples from children with an acute wheezing episode (n=373, 0-16 years of age), with RV-C the most common virus (65.5%). Children with a history of parental asthma and/or allergy and RV at recruitment had a 14-fold increased incidence rate ratio (IRR) of subsequent RV detection (IRR 14.0, 95% CI 1.9-104.1; p=0.01) compared with children without RV at recruitment. Children without this parental history had a reduced incident rate ratio for samples assessed during this time (IRR 0.5, 95% CI 0.3-0.9; p=0.03). CONCLUSION Children with a parental history of asthma and/or allergy may become more susceptible to recurrent symptomatic RV infections.

Collaboration


Dive into the S. Khoo's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar

J. Goldblatt

Princess Margaret Hospital for Children

View shared research outputs
Top Co-Authors

Avatar

Joelene Bizzintino

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

P. N. Le Souëf

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

Catherine M. Hayden

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

Ia Laing

University of Western Ontario

View shared research outputs
Top Co-Authors

Avatar

Ingrid A. Laing

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

Jack Goldblatt

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

Pierre Candelaria

University of Western Australia

View shared research outputs
Top Co-Authors

Avatar

Vibeke Backer

University of Copenhagen

View shared research outputs
Researchain Logo
Decentralizing Knowledge