A nonself sugar mimic of the HIV glycan shield shows enhanced antigenicity

Antibody 2G12 uniquely neutralizes a broad range of HIV-1 isolates by binding the high-mannose glycans on the HIV-1 surface glycoprotein, gp120. Antigens that resemble these natural epitopes of 2G12 would be highly desirable components for an HIV-1 vaccine. However, host-produced (self)-carbohydrate motifs have been unsuccessful so far at eliciting 2G12-like antibodies that cross-react with gp120. Based on the surprising observation that 2G12 binds nonproteinaceous monosaccharide D-fructose with higher affinity than D-mannose, we show here that a designed set of nonself, synthetic monosaccharides are potent antigens. When introduced to the terminus of the D1 arm of protein glycans recognized by 2G12, their antigenicity is significantly enhanced. Logical variation of these unnatural sugars pinpointed key modifications, and the molecular basis of this increased antigenicity was elucidated using high-resolution crystallographic analyses. Virus-like particle protein conjugates containing such nonself glycans are bound more tightly by 2G12. As immunogens they elicit higher titers of antibodies than those immunogenic conjugates containing the self D1 glycan motif. These antibodies generated from nonself immunogens also cross-react with this self motif, which is found in the glycan shield, when it is presented in a range of different conjugates and glycans. However, these antibodies did not bind this glycan motif when present on gp120.     

A 1-year prospective study of the infectious etiology in patients hospitalized with acute exacerbations of COPD

INTRODUCTION: Infection is a major cause of acute exacerbations of COPD (AECOPDs). We aimed to study the infectious etiology related to AECOPD. METHODS: Patients admitted to an acute care hospital in Hong Kong with an AECOPD were recruited prospectively from May 1, 2004, to April 30, 2005. Sputum samples, nasopharyngeal aspirate (NPA) samples, and paired serology specimens were collected. Spirometry was performed with patients in the stable phase 2 to 3 months after hospital discharge. RESULTS: There were 643 episodes of AECOPD among 373 patients. Their mean age was 75.3 years (SD, 7.9 years) with 307 male patients. The mean FEV(1) was 40.4% predicted (SD, 18.7% predicted), and the mean FEV(1)/FVC ratio was 58.4% (SD, 16.0%). Among sputum samples from the 530 episodes of AECOPD hospital admissions that were saved, 13.0%, 6.0%, and 5.5%, respectively, had positive growth of Haemophilus influenzae, Pseudomonas aeruginosa, and Streptococcus pneumoniae. Among the 505 hospital admissions with patients who had NPA samples saved, 5.7%, 2.3%, 0.8%, and 0.8%, respectively, had influenza A, respiratory syncytial virus (RSV), influenza B, and parainfluenza 3 isolated from viral cultures. Paired serology test results revealed a fourfold rise in viral titers in 5.2%, 2.2%, and 1.4% of patients, respectively, for influenza A, RSV, and influenza B. Very severe airflow obstruction (stable-state spirometry) was associated with a higher chance of a positive sputum culture (FEV(1) >/= 30% predicted, 28.2%; FEV(1) < 30% predicted, 40.4%; p = 0.006). CONCLUSION: H influenzae and influenza A were the most common etiologic agents in patients who were hospitalized with AECOPDs. More severe airflow obstruction was associated with a higher chance of a positive sputum culture finding.     

Oxygen toxicity

The “free radical theory of oxygen toxicity” attributes the damaging effects of hyperoxia to highly-reactive metabolic products of oxygen (O₂) that can inactivate enzymes in the cell, damage DNA and destroy lipid membranes. To protect the organism from these cytotoxic O₂ metabolites, an array of cooperative antioxidant defense systems have evolved. These include the enzyme superoxide dismutase (SOD), catalase and glutathione peroxidase, plus other endogenous antioxidants such as ascorbate and vitamin E. The increased levels of O₂-free radicals produced during hyperoxia may overwhelm these normal antioxidant defense systems. The ability to respond rapidly to hyperoxic challenge with increased antioxidant activity has been shown repeatedly to be associated with relative tolerance to O₂-induced injury and lethality.Treatment with exogenous SOD or vitamin E has had some clinical success in combating O₂-free radical-mediated tissue injury. Treatment with small doses of bacterial endotoxin has provided almost complete protection to rats against pulmonary O₂ toxicity; this agent seems to act by facilitating rapid increases in endogenous antioxidant enzyme levels.An increased understanding of the molecular mechanisms of O₂ toxicity and of the endogenous defenses that organisms have evolved against O₂-free radical injury may lead to a more rational basis for the clinical use of O₂ and to the development of therapeutic measures effective in preventing or ameliorating O₂ toxicity. These measures may involve (1) tests aimed at estimating a person's tolerance to hyperoxia at any given time, (2) means to effectively deliver exogenous antioxidants and (3) methods to augment endogenous antioxidant defenses.     

Plasma luteinizing hormone in male ring doves during the breeding cycle

Plasma levels of LH were analyzed in male ring doves throughout a breeding cycle. LH levels were low in visually isolated animals [(8.0 ± 1.6 ng/ml) (X ± SE)], peaked the day after pairing with a female (14.3 ± 2.52 ng/ml), and declined to baseline levels during incubation and brooding. If eggs or squab were removed during the period of parental care, LH levels rose. The increase in LH following removal of eggs was more prolonged in late incubation than in early incubation. We conclude that the female enhances while the young (eggs or squab) suppress LH in male ring doves.     

Preclinical pharmacology and antitumour activity of the novel sequence-selective DNA minor-groove cross-linking agent DSB-120

 We examined the in vitro cytotoxicity, antitumour activity and preclinical pharmacokinetics of the novel sequence-selective, bifunctional alkylating agent DSB-120, a synthetic pyrrolo[1, 4][2, 1-c]benzodiazepine dimer. DSB-120 was shown to be a potent cytotoxic agent in vitro against a panel of human colon carcinomas [50% growth-inhibitory concentration (IC₅₀) 42±7.9 nM, mean±SE, n=7] and two rodent tumours (L1210 and ADJ/PC6). Antitumour activity was assessed in the bifunctional alkylating-agent-sensitive murine plasmacytoma ADJ/PC6 using a variety of administration protocols. The maximal antitumour eff- ects were observed following a single i.v. dose but the therapeutic index was only 2.6. DSB-120 was less effective when given i.p. either singly or by a daily+5 schedule. After a single i.v. dose at the maximum tolerated dose (MTD, 5 mg kg⁻¹) the plasma elimination was biphasic, with a short distribution phase (t _1/2α 4 min) being followed by a longer elimination phase (t _1/3β 38 min). Peak plasma concentrations were 25 μg ml⁻¹, the clearance was 1.3 ml g⁻¹ h⁻¹ and the AUC_0-∞ was 230 μg ml⁻¹ min. Concentrations of DSB-120 in ADJ/PC6 tumours were very low, showing a peak of 0.4 μg g⁻¹at 5 min. The steady-state tumour/plasma ratio was about 5% and the AUC was only 2.5% of that occurring in the plasma. DSB-120 appeared to be unstable in vivo, with only 1% of an administered dose being recovered unchanged in 24-h urine samples. Plasma protein binding was extensive at 96.6%. In conclusion, the poor antitumour activity of DSB-120 may be a consequence of low tumour selectivity and drug uptake as a result of high protein binding and/or extensive drug metabolism in vivo. Received: 5 November 1995/Accepted: 30 January 1996     

Association between daily walking and antioxidant capacity in patients with symptomatic peripheral artery disease

Objective

The primary aim of the study was to assess whether both the amount and pace of daily walking were associated with circulating antioxidant capacity in symptomatic patients with peripheral artery disease (PAD).

Lobular Carcinoma In Situ

Lobular carcinoma in situ (LCIS) is a risk factor and a nonobligate precursor of breast carcinoma. The relative risk of invasive carcinoma after classic LCIS diagnosis is approximately 9 to 10 times that of the general population. Classic LCIS diagnosed on core biopsy with concordant imaging and pathologic findings does not mandate surgical excision, and margin status is not reported. The identification of variant LCIS in a needle core biopsy specimen mandates surgical excision, regardless of radiologic-pathologic concordance. The presence of variant LCIS close to the surgical margin of a resection specimen is reported, and reexcision should be considered.