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  1. AU="Hand, Marissa"
  2. AU="Guerra, Giselle"
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  1. Article ; Online: Outcomes after extended azithromycin administration in preterm premature rupture of membranes.

    DiSciullo, Alison J / Hand, Marissa / Iqbal, Sara N / Chornock, Rebecca L

    AJOG global reports

    2023  Volume 3, Issue 2, Page(s) 100206

    Abstract: Background: Preterm premature rupture of membranes accounts for approximately one-quarter of all preterm deliveries and occurs in 2% to 3% of all pregnancies. With subclinical infection being a suspected cause of preterm premature rupture of membranes, ... ...

    Abstract Background: Preterm premature rupture of membranes accounts for approximately one-quarter of all preterm deliveries and occurs in 2% to 3% of all pregnancies. With subclinical infection being a suspected cause of preterm premature rupture of membranes, the administration of prophylactic antibiotics is an accepted standard of care to extend the latency period. Historically, erythromycin was used in the antibiotic regimen recommended for women with preterm premature rupture of membranes during expectant management; however, azithromycin has recently been shown to be a suitable alternative.
    Objective: This study aimed to evaluate whether extended azithromycin administration affects the latency time in preterm premature rupture of membranes.
    Study design: This was a retrospective multi-institutional cohort study in Washington, District of Columbia, of patients admitted from January 2012 to December 2019 with preterm premature rupture of membranes of singleton pregnancies between 23 0/7 and 33 6/7 weeks of gestation. Patients were excluded if they had multiple pregnancies, had an allergy to penicillin or macrolides, were in labor, had suspected placental abruptions, had overt chorioamnionitis, or had nonreassuring fetal status on presentation indicating the need for prompt delivery. Patients that received limited azithromycin administration (<2 days) and patients that received extended azithromycin administration (7 days) were compared. All patients otherwise received the institutional standard of 2 days of intravenous ampicillin followed by 5 days of oral amoxicillin. The primary outcome was length of gestational latency, defined as the time from membrane rupture to delivery. The selective secondary outcomes that were evaluated were rates of chorioamnionitis and adverse neonatal outcomes, including sepsis, respiratory distress, necrotizing enterocolitis, intraventricular hemorrhage, and neonatal death.
    Results: During the study period, 416 cases of preterm premature rupture of membranes were identified. Of the 287 patients who met the inclusion criteria, 165 (57.5%) received limited azithromycin administration, and 122 (42.5%) received extended azithromycin administration. Adjusted median gestational latency was significantly longer for patients who received extended azithromycin administration, extended by >3 days (2.6 days [interquartile range, 2.2-3.1] for limited azithromycin administration vs 5.8 days [interquartile range, 4.8-6.9] for extended azithromycin administration;
    Conclusion: Among patients with preterm premature rupture of membranes, extended azithromycin administration was associated with increased latency, without any effect on other maternal or neonatal outcomes.
    Language English
    Publishing date 2023-04-05
    Publishing country United States
    Document type Journal Article
    ISSN 2666-5778
    ISSN (online) 2666-5778
    DOI 10.1016/j.xagr.2023.100206
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Lipid-dependent regulation of exocytosis in

    Smindak, Richard J / Heckle, Lindsay A / Chittari, Supraja S / Hand, Marissa A / Hyatt, Dylan M / Mantus, Grace E / Sanfelippo, William A / Kozminski, Keith G

    Journal of cell science

    2017  Volume 130, Issue 22, Page(s) 3891–3906

    Abstract: Polarized exocytosis is an essential process in many organisms and cell types for correct cell division or functional specialization. Previous studies established that homologs of the oxysterol-binding protein (OSBP) ... ...

    Abstract Polarized exocytosis is an essential process in many organisms and cell types for correct cell division or functional specialization. Previous studies established that homologs of the oxysterol-binding protein (OSBP) in
    Language English
    Publishing date 2017-11-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 2993-2
    ISSN 1477-9137 ; 0021-9533
    ISSN (online) 1477-9137
    ISSN 0021-9533
    DOI 10.1242/jcs.205435
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: IgG3 regulates tissue-like memory B cells in HIV-infected individuals.

    Kardava, Lela / Sohn, Haewon / Youn, Christine / Austin, James W / Wang, Wei / Buckner, Clarisa M / Justement, J Shawn / Melson, Valerie A / Roth, Gwynne E / Hand, Marissa A / Gittens, Kathleen R / Kwan, Richard W / Sneller, Michael C / Li, Yuxing / Chun, Tae-Wook / Sun, Peter D / Pierce, Susan K / Moir, Susan

    Nature immunology

    2018  Volume 19, Issue 9, Page(s) 1001–1012

    Abstract: Immunoglobulin G3 (IgG3) has an uncertain role in the response to infection with and vaccination against human immunodeficiency virus (HIV). Here we describe a regulatory role for IgG3 in dampening the immune system-activating effects of chronic HIV ... ...

    Abstract Immunoglobulin G3 (IgG3) has an uncertain role in the response to infection with and vaccination against human immunodeficiency virus (HIV). Here we describe a regulatory role for IgG3 in dampening the immune system-activating effects of chronic HIV viremia on B cells. Secreted IgG3 was bound to IgM-expressing B cells in vivo in HIV-infected chronically viremic individuals but not in early-viremic or aviremic individuals. Tissue-like memory (TLM) B cells, a population expanded by persistent HIV viremia, bound large amounts of IgG3. IgG3 induced clustering of B cell antigen receptors (BCRs) on the IgM
    MeSH term(s) Adult ; B-Lymphocytes/immunology ; C-Reactive Protein/metabolism ; Cells, Cultured ; Complement C1q/metabolism ; Female ; HIV Infections/immunology ; HIV-1/physiology ; Humans ; Immunoglobulin G/metabolism ; Immunoglobulin M/metabolism ; Immunologic Memory ; Immunomodulation ; Male ; Middle Aged ; Protein Binding ; Receptor Aggregation ; Receptors, Antigen, B-Cell/metabolism ; Receptors, IgG/metabolism ; Young Adult
    Chemical Substances Fc gamma receptor IIB ; Immunoglobulin G ; Immunoglobulin M ; Receptors, Antigen, B-Cell ; Receptors, IgG ; Complement C1q (80295-33-6) ; C-Reactive Protein (9007-41-4)
    Language English
    Publishing date 2018-08-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Intramural
    ZDB-ID 2016987-5
    ISSN 1529-2916 ; 1529-2908
    ISSN (online) 1529-2916
    ISSN 1529-2908
    DOI 10.1038/s41590-018-0180-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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