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1.
MMWR Morb Mortal Wkly Rep ; 72(20): 559-563, 2023 May 19.
Article in English | MEDLINE | ID: mdl-37339074

ABSTRACT

In 2022, an international Monkeypox virus outbreak, characterized by transmission primarily through sexual contact among gay, bisexual, and other men who have sex with men (MSM), resulted in 375 monkeypox (mpox) cases in the state of New York outside of New York City (NYC).*,† The JYNNEOS vaccine (Modified Vaccinia Ankara vaccine, Bavarian Nordic), licensed by the U.S. Food and Drug Administration (FDA) against mpox as a 2-dose series, with doses administered 4 weeks apart,§ was deployed in a national vaccination campaign.¶ Before this outbreak, evidence to support vaccine effectiveness (VE) against mpox was based on human immunologic and animal challenge studies (1-3). New York State Department of Health (NYSDOH) conducted a case-control study to estimate JYNNEOS VE against diagnosed mpox in New York residents outside of NYC, using data from systematic surveillance reporting. A case-patient was defined as a man aged ≥18 years who received a diagnosis of mpox during July 24-October 31, 2022. Contemporaneous control patients were men aged ≥18 years with diagnosed rectal gonorrhea or primary syphilis and a history of male-to-male sexual contact, without mpox. Case-patients and control patients were matched to records in state immunization systems. JYNNEOS VE was estimated as 1 - odds ratio (OR) x 100, and JYNNEOS vaccination status (vaccinated versus unvaccinated) at the time of diagnosis was compared, using conditional logistic regression models that adjusted for week of diagnosis, region, patient age, and patient race and ethnicity. Among 252 eligible mpox case-patients and 255 control patients, the adjusted VE of 1 dose (received ≥14 days earlier) or 2 doses combined was 75.7% (95% CI = 48.5%-88.5%); the VE for 1 dose was 68.1% (95% CI = 24.9%-86.5%) and for 2 doses was 88.5% (95% CI = 44.1%-97.6%). These findings support recommended 2-dose JYNNEOS vaccination consistent with CDC and NYSDOH guidance.


Subject(s)
Antiviral Agents , Mpox (monkeypox) , Smallpox Vaccine , Adolescent , Adult , Animals , Female , Humans , Male , Case-Control Studies , Homosexuality, Male , Mpox (monkeypox)/diagnosis , Mpox (monkeypox)/prevention & control , New York City/epidemiology , Sexual and Gender Minorities , United States , Vaccines , Antiviral Agents/administration & dosage , Smallpox Vaccine/administration & dosage , Vaccines, Attenuated/administration & dosage
3.
Sex Transm Dis ; 48(8S): S40-S43, 2021 08 01.
Article in English | MEDLINE | ID: mdl-33967232

ABSTRACT

ABSTRACT: This evaluation describes an increase in reported drug-related risk behaviors among females who are diagnosed with early syphilis over a 5-year span in New York State, excluding New York City. Integrating sexually transmitted infection prevention efforts with harm reduction services may help decrease syphilis rates in areas where drug-related risk behavior rates are high.


Subject(s)
HIV Infections , Pharmaceutical Preparations , Sexually Transmitted Diseases , Syphilis , Female , Humans , New York City/epidemiology , Risk-Taking , Sexually Transmitted Diseases/diagnosis , Sexually Transmitted Diseases/epidemiology , Syphilis/diagnosis , Syphilis/epidemiology
4.
Sex Transm Dis ; 48(5): 381-384, 2021 05 01.
Article in English | MEDLINE | ID: mdl-33534404

ABSTRACT

ABSTRACT: During the initial height of COVID-19 in New York State excluding New York City in March 2020, reports of sexually transmitted infections declined. Prediction models developed to estimate the incidence of early syphilis and gonorrhea during the COVID-19 pandemic were used to study impact on STI diagnoses/reporting and inform sexual health program planning.


Subject(s)
COVID-19 , Models, Theoretical , Sexually Transmitted Diseases/epidemiology , Gonorrhea/epidemiology , Humans , Incidence , New York/epidemiology , Pandemics , Syphilis/epidemiology
5.
Obstet Gynecol ; 128(1): 44-51, 2016 07.
Article in English | MEDLINE | ID: mdl-27275796

ABSTRACT

OBJECTIVE: To identify factors associated with continuity of care and human immunodeficiency virus (HIV) virologic suppression among postpartum women diagnosed with HIV during pregnancy in New York State. METHODS: This retrospective cohort study was conducted among 228 HIV-infected women diagnosed during pregnancy between 2008 and 2010. Initial receipt of HIV-related medical care (first CD4 or viral load test after diagnosis) was evaluated at 30 days after diagnosis and before delivery. Retention in care (2 or more CD4 or viral load tests, 90 days or greater apart) and virologic suppression (viral load 200 copies/mL or less) were evaluated in the 12 months after hospital discharge. RESULTS: Most women had their initial HIV-related care encounter within 30 days of diagnosis (74%) and before delivery (87%). Of these women, 70% were retained in the first year postpartum. Women waiting more than 30 days for their initial HIV-related care encounter were more likely diagnosed in the first (29%) compared with the third (11%) trimester and were of younger (younger than 25 years, 32%) compared with older (35 years or older, 13%) age. Loss to follow-up within the first year was significantly greater among women diagnosed in the third compared with the first trimester (adjusted relative risk 2.21, 95% confidence interval [CI] 1.41-3.45) and among women who had a cesarean compared with vaginal delivery (adjusted relative risk 1.76, 95% CI 1.07-2.91). Of the 178 women with one or more HIV viral load test in the first year postpartum, 58% had an unsuppressed viral load. CONCLUSION: Despite the high proportion retained in care, many women had poor postpartum virologic control. Robust strategies are needed to increase virologic suppression among newly diagnosed postpartum HIV-infected women.


Subject(s)
HIV Infections , Postnatal Care , Pregnancy Complications, Infectious , Viral Load , Adult , Age Factors , CD4 Lymphocyte Count , Female , HIV Infections/blood , HIV Infections/diagnosis , HIV Infections/epidemiology , Humans , Lost to Follow-Up , New York/epidemiology , Postnatal Care/methods , Postnatal Care/organization & administration , Postpartum Period/blood , Pregnancy , Pregnancy Complications, Infectious/blood , Pregnancy Complications, Infectious/diagnosis , Pregnancy Complications, Infectious/epidemiology , Retrospective Studies , Risk Factors , Viral Load/methods , Viral Load/statistics & numerical data
6.
J Infect Dis ; 214(2): 182-8, 2016 07 15.
Article in English | MEDLINE | ID: mdl-26740276

ABSTRACT

BACKGROUND: In the northeastern United States, tick-borne diseases are a major public health concern. In controlled studies, a single springtime application of acaricide has been shown to kill 68%-100% of ticks. Although public health authorities recommend use of acaricides to control tick populations in yards, the effectiveness of these pesticides to prevent tick bites or human tick-borne diseases is unknown. METHODS: We conducted a 2-year, randomized, double-blinded, placebo-controlled trial among 2727 households in 3 northeastern states. Households received a single springtime barrier application of bifenthrin or water according to recommended practices. Tick drags were conducted 3-4 weeks after treatment on 10% of properties. Information on human-tick encounters and tick-borne diseases was collected through monthly surveys; reports of illness were validated by medical record review. RESULTS: Although the abundance of questing ticks was significantly lower (63%) on acaricide-treated properties, there was no difference between treatment groups in human-tick encounters, self-reported tick-borne diseases, or medical-record-validated tick-borne diseases. CONCLUSIONS: Used as recommended, acaricide barrier sprays do not significantly reduce the household risk of tick exposure or incidence of tick-borne disease. Measures for preventing tick-borne diseases should be evaluated against human outcomes to confirm effectiveness.


Subject(s)
Acaricides/administration & dosage , Tick Bites/prevention & control , Tick-Borne Diseases/prevention & control , Ticks/drug effects , Ticks/growth & development , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Child , Child, Preschool , Double-Blind Method , Family Characteristics , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , New England , Placebos/administration & dosage , Pyrethrins/administration & dosage , Tick Bites/epidemiology , Tick-Borne Diseases/epidemiology , Young Adult
7.
Pediatrics ; 133(3): e494-504, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24515517

ABSTRACT

OBJECTIVES: To estimate tuberculosis (TB) rates among young children in the United States by children's and parents' birth origins and describe the epidemiology of TB among young children who are foreign-born or have at least 1 foreign-born parent. METHODS: Study subjects were children <5 years old diagnosed with TB in 20 US jurisdictions during 2005-2006. TB rates were calculated from jurisdictions' TB case counts and American Community Survey population estimates. An observational study collected demographics, immigration and travel histories, and clinical and source case details from parental interviews and health department and TB surveillance records. RESULTS: Compared with TB rates among US-born children with US-born parents, rates were 32 times higher in foreign-born children and 6 times higher in US-born children with foreign-born parents. Most TB cases (53%) were among the 29% of children who were US born with foreign-born parents. In the observational study, US-born children with foreign-born parents were more likely than foreign-born children to be infants (30% vs. 7%), Hispanic (73% vs. 37%), diagnosed through contact tracing (40% vs. 7%), and have an identified source case (61% vs. 19%); two-thirds of children were exposed in the United States. CONCLUSIONS: Young children who are US born of foreign-born parents have relatively high rates of TB and account for most cases in this age group. Prompt diagnosis and treatment of adult source cases, effective contact investigations prioritizing young contacts, and targeted testing and treatment of latent TB infection are necessary to reduce TB morbidity in this population.


Subject(s)
Emigrants and Immigrants , Population Surveillance/methods , Tuberculosis/diagnosis , Tuberculosis/epidemiology , Child, Preschool , Cross-Sectional Studies , Female , Humans , Male , Risk Factors , United States/epidemiology
8.
Am J Physiol Cell Physiol ; 283(3): C950-9, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12176751

ABSTRACT

Neonatal sciatic nerve crush results in a sustained reduction of the mass of both extensor digitorum longus (EDL) and soleus (SOL) muscles in the rat. Type IIB fibers are selectively lost from EDL. We have investigated the effects of ciliary neurotrophic factor (CNTF) combined with neurotrophin (NT)-3 or NT-4 on muscle mass, as well as the number, cross-sectional area, and distribution of muscle fiber types and the number of motor neurons innervating EDL and SOL 3 mo after transient axotomy 5 days after birth. Both NT treatments prevented the axotomy-induced loss of muscle mass in both EDL and SOL and of total number of muscle fibers in EDL but not in SOL. Although IIB fiber loss was not prevented, both NT treatments resulted in altered fiber type distribution. Both NT combinations also reduced the loss of EDL motor neurons. These data suggest that a differential distribution of NT receptors on either motor neurons or muscle fibers may lead to different levels of susceptibility to neonatal axotomy.


Subject(s)
Muscle Fibers, Skeletal/drug effects , Muscle, Skeletal/drug effects , Nerve Growth Factors/pharmacology , Sciatic Neuropathy/drug therapy , Animals , Animals, Newborn , Axotomy , Cell Survival/drug effects , Ciliary Neurotrophic Factor/pharmacology , Disease Models, Animal , Drug Therapy, Combination , Immunohistochemistry , Motor Neurons/drug effects , Motor Neurons/pathology , Muscle Contraction/drug effects , Muscle Contraction/physiology , Muscle Fibers, Skeletal/classification , Muscle Fibers, Skeletal/pathology , Muscle, Skeletal/innervation , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Myosin Heavy Chains/biosynthesis , Nerve Crush , Neurotrophin 3/pharmacology , Rats , Rats, Sprague-Dawley , Sciatic Neuropathy/pathology , Sciatic Neuropathy/physiopathology
9.
Development ; 129(11): 2591-606, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12015288

ABSTRACT

We establish that the jing zinc-finger transcription factor plays an essential role in controlling CNS midline and tracheal cell differentiation. jing transcripts and protein accumulate from stage 9 in the CNS midline, trachea and in segmental ectodermal stripes. JING protein localizes to the nuclei of CNS midline and tracheal cells implying a regulatory role during their development. Loss of jing-lacZ expression in homozygous sim mutants and induction of jing-lacZ by ectopic sim expression establish that jing is part of the CNS midline lineage. We have isolated embryonic recessive lethal jing mutations that display genetic interactions in the embryonic CNS midline and trachea, with mutations in the bHLH-PAS genes single-minded and trachealess, and their downstream target genes (slit and breathless). Loss- and gain-of-function jing is associated with defects in CNS axon and tracheal tubule patterning. In jing homozygous mutant embryos, reductions in marker gene expression and inappropriate apoptosis in the CNS midline and trachea establish that jing is essential for the proper differentiation and survival of these lineages. These results establish that jing is a key component of CNS midline and tracheal cell development. Given the similarities between JING and the vertebrate CCAAT-binding protein AEBP2, we propose that jing regulates transcriptional mechanisms in Drosophila embryos and promotes cellular differentiation in ectodermal derivatives.


Subject(s)
Body Patterning/physiology , Drosophila Proteins , Drosophila melanogaster/embryology , Gene Expression Regulation, Developmental , Nuclear Proteins/genetics , Trachea/embryology , Transcription Factors/genetics , Animals , Aryl Hydrocarbon Receptor Nuclear Translocator , Basic Helix-Loop-Helix Transcription Factors , Carrier Proteins/genetics , Cell Differentiation , DNA-Binding Proteins/genetics , Drosophila melanogaster/genetics , Embryo, Nonmammalian/physiology , Ethyl Methanesulfonate , Female , Genes, Lethal , Genes, Recessive , Helix-Loop-Helix Motifs , Insect Proteins/genetics , Mutagenesis , Nuclear Proteins/analysis , Nuclear Proteins/metabolism , Ovary/embryology , Phenotype , Transcription Factors/analysis , Transcription Factors/metabolism , Zinc Fingers
10.
Biochim Biophys Acta ; 1054(3): 311-6, 1990 Sep 24.
Article in English | MEDLINE | ID: mdl-2207180

ABSTRACT

The chronic administration of isoproterenol ((+-)-1-(3,4)-dihydroxyphenyl)-2-isopropylaminoethanol) induces both the accumulation of a family of secretory polypeptides (polypeptides C, D, E, F and G) and growth in size in mouse parotid glands. Eleven isoproterenol analogs including minor structural modifications either at the aromatic ring, at the ethanol-derived residue or at the end group bonded to the amino of the side chain, were analysed regarding their ability to produce those two responses. Analogs were distributed into two groups, namely inducers and noninducers. Inducer isoproterenol analogs provoked a massive accumulation of polypeptides C, D, E, F and G and were active in producing parotid gland enlargement. Noninducer isoproterenol analogs produced neither changes in the polypeptide composition nor growth response in these glands. Thus, a correlation between accumulation of polypeptides C, D, E, F and G and the growth in size response in parotid glands was more firmly established. In considering the chemical structure of the isoproterenol analogs with regard to their inducer or noninducer character, the three main domains taken into account appeared to participate in the inductive process. However, while an intact ethanol-derived domain was found to be absolutely necessary for the inductive ability of the analogs, both the aromatic ring as well as the substituent on the side-chain amino group could experience several modifications without resulting in loss of the inductive character.


Subject(s)
Isoproterenol/analogs & derivatives , Parotid Gland/metabolism , Salivary Proteins and Peptides/metabolism , Animals , Electrophoresis, Polyacrylamide Gel , Isoproterenol/pharmacology , Male , Mice , Mice, Inbred Strains , Molecular Weight , Organ Size/drug effects , Parotid Gland/drug effects , Parotid Gland/growth & development , Salivary Proteins and Peptides/chemistry , Structure-Activity Relationship
13.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.57-62, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871896
15.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.115-28, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871898
16.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.237-42, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871903
17.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.243-51, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871904
18.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.261-74, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871906
20.
In. Miranda, Claudio Cezar de. Atlas de reabilitaçäo bucal. Säo Paulo, Santos, 1988. p.523-9, ilus.
Monography in Portuguese | LILACS, BBO - Dentistry | ID: biblio-871913
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